User Manual ERBEJET - 2

USER MANUAL
ERBEJET® 2
V 1.1.x
HYDROSURGERY 80110-801 2019-01

USER MANUAL
ERBEJET® 2
Registered trademarks of Erbe Elektromedizin GmbH: AUTO CUT®, AXUS®, BICISION®, BiClamp®, classicCOAG®, classicCUT®,
CLEVERCAP®, DeCo®, dryCUT®, endoCUT®, endoCOAG®, ERBE®, erbe power your performance.®, ERBECRYO®, ERBEFLO®,
ERBEFLO AeroRinse®, ERBEJET®, ERBELift®, ERBOKRYO®, FIAPC®, forcedCOAG®, Hybrid knife®, HybridKnife®, ICC 200®,
ICC 80®, KYRON®, NESSY®, NESSY Ω®, PLURA®, preciseAPC®, Preflow®, pulsedAPC®, ReMode®, REMODE®, softCOAG®,
sprayCOAG®, swiftCOAG®, The Color Blue®, thermoSEAL®, twinCOAG®, VIO®.
MEDICAL - GENERAL MEDICAL EQUIPMENT

AS TO ELECTRICAL SHOCK, FIRE
AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH
ANSI/AAMI ES60601-1 (2005),
CAN/CSA-C22.2 No. 60601-1 (2008)
19NA
CE0124
User Manual Art. No. 80110-801
Product Art. No. 10150-000
All rights to this User Manual, in particular rights of duplication, dissemination and translation, are reserved. No part of this User
Manual may be reproduced in any form (by photocopying, microfilming or other methods) or processed, duplicated or dissemi-
nated by the use of electronic systems without the written consent of Erbe Elektromedizin GmbH.
The information contained in this User Manual can be changed or expanded without prior notice and without obligation on the
part of Erbe Elektromedizin GmbH.
Printed by Erbe Elektromedizin
Printed in Germany
Copyright © Erbe Elektromedizin GmbH, Tübingen 2019
Table of Contents
Table of Contents
1 Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Intended use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Safety notations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Meaning of the note. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Who must read this User Manual? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Compliance with safety information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Structure of safety instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Operating errors and incorrect installation by persons without training . . . . . . . . . . 8
Risks due to the environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Electric shock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Risk of infection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Fire / explosion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Defective unit, defective accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Interference caused by the unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Safety information for use of ERBEJET 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
2 Description of the Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

Controls on the front panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Controls on the back . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
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3 Working with ERBEJET 2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

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Connecting suction module ESM 2, connecting the applicator to the pump

unit, replacing the applicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Selecting program, Inserting pump unit, Connecting separating medium,
Priming pump unit and applicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Mounting suction hose of applicator to suction container . . . . . . . . . . . . . . . . . . . . 26
Window settings, Selecting effect, Setting suction . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Activation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Saving a modified basic program as a new program, Selecting program,
Saving programs for the ReMode function. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Deleting a program, Overwriting a program. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
ml-Signal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Displaying used separating medium, Resetting display . . . . . . . . . . . . . . . . . . . . . . 34
Having the unit of pressure set. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Accessing Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
4 Status Messages, Error Messages . . . . . . . . . . . . . . . . . . . . . . . . . . 37

Status messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Error messages. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Error messages with error codes in numerical order. . . . . . . . . . . . . . . . . . . . . . . . . 38
Error messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
5 Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Ambient conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
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Table of Contents
Electrical installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43

Installing ERBEJET 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
6 Disassembly, Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . 45

Removal of separating medium; disassembly of ESM 2 suction unit,
applicator, and pump unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .45
Wipe disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .46
Instructions for cleaning and disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .47
7 Technical Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
8 Information on electromagnetic compatibility (EMC) . . . . . . . . . . . 51
9 Maintenance, Customer Service, Warranty, Disposal . . . . . . . . . . . . 55

Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55
Customer service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55
Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55
Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .56
10 Combination with other equipment, Third-party accessories . . . . . 57
11 Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .59
ERBEJET 2 example accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .60
12 Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
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1 • Safety Instructions
Chapter 1
Safety Instructions
Intended use
The ERBEJET 2 water jet surgical unit is intended for applying a high pressure water
jet. The water jet can be used for marking, rinsing, lifting and dissecting tissues.
Safety notations
DANGER
indicates an imminently hazardous situation which, if not avoided,
will result in death or serious injury.
WARNING
indicates a potentially hazardous situation which, if not avoided,
could result in death or serious injury.
CAUTION
indicates a potentially hazardous situation which, if not avoided, may
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result in minor or moderate injury.
NOTICE
indicates a potentially hazardous situation which, if not avoided, may
result in property damage.
Meaning of the note

"Note:"
Refers a) to manufacturer's information that relates directly or indirectly to the safety
of people or protection of property. The information does not relate directly to a risk
or dangerous situation.
Refers b) to manufacturer's information that is important or useful for operating or
servicing the unit.
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Who must read this User Manual?

Knowledge of the User Manual is absolutely essential for correct operation of the unit.
The User Manual must therefore be read by everyone who works with the equipment.
Anyone who prepares, sets, disassembles, cleans and disinfects the unit must also
read the User Manual.
Please pay particular attention to the safety instructions in each chapter.
Compliance with safety information

Working with medical equipment is associated with certain risks to patients, medical
personnel and the environment. Risks cannot be entirely eliminated by design mea-
sures alone.
Safety does not depend solely on the equipment. Safety depends to a large extent on
the training of medical personnel and correct operation of the equipment.
The safety instructions in this chapter must be read, understood and applied by every-
one who is working with the equipment.
Structure of safety instructions

The safety instructions are structured according to the following risks:
• Operating errors and incorrect installation by persons without training
• Risks due to the environment
• Electric shock
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• Risk of infection
• Fire / explosion
• Defective unit, defective accessories
• Interference caused by the unit
• Safety information for use of ERBEJET 2
• Notes
Operating errors and incorrect installation by persons without training
WARNING
Operating errors and incorrect installation by persons without
training
Persons without training can operate or install the unit incorrectly.
Risk of injury or death for patients and medical staff! Risk of damage
to property.
 The equipment may only be used and installed by persons who
have been trained on how to use and install it properly according
to this User Manual.
 Training may only be carried out by persons who are suitable on
the basis of their knowledge and practical experience.
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 In the event of uncertainties or if you have any questions, please

contact Erbe Elektromedizin. You will find the addresses in the ad-
dress list at the end of this User Manual.
Risks due to the environment
NOTICE
Interference with the unit from portable and mobile HF telecom-
munications equipment (e.g. mobile phones, WLAN equipment)
Electromagnetic waves emitted by portable and mobile HF telecom-
munications equipment may affect the unit.
The unit may fail or not perform properly.
 When using portable and mobile HF telecommunications devices,
including their accessories, there must be a distance of at least
30 cm between them and the device and its cords.
NOTICE
Unsuitable temperature or level of humidity during operation
If you operate the equipment at an unsuitable temperature or level of
humidity, it may sustain damage, fail, or not perform properly.
 Operate the equipment at a suitable temperature and level of hu-
midity. You will find the tolerances for temperature and humidity
in the Technical Data.
 If other ambient conditions must be observed for operation of the
equipment, you will also find them in the Technical Data.
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NOTICE
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Unsuitable temperature or humidity in transit or storage

If you transport or store the equipment at an unsuitable temperature
or level of humidity, it may sustain damage and fail.
 Transport and store the equipment at a suitable temperature and
level of humidity. You will find the tolerances for temperature and
humidity in the Technical Data.
 If other ambient conditions must be observed for transport and
storage of the equipment, you will also find them in the Technical
Data.
NOTICE
Insufficient acclimatization time, unsuitable temperature during
acclimatization
If the device was stored or transported below or above a certain tem-
perature, it will take a certain time and temperature to acclimatize.
If you do not observe the rules, the device can sustain damage and
fail.
 Acclimatize the device according to the rules in the Technical Da-
ta.
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NOTICE
Overheating of the device due to poor ventilation
If ventilation is poor, the device can overheat, sustain damage, and fail.
 Install the device in such a way that there is an unobstructed cir-
culation of air around the housing. Installation in confined wall re-
cesses is prohibited.
NOTICE
Penetration of liquid into the device
The housing is not absolutely watertight. If liquid penetrates, the de-
vice can sustain damage and fail.
 Make sure no liquid can penetrate the device.
 Do not place vessels containing liquids on top of the device.
 Take care when connecting the separating medium to the pump
unit that the unit does not come into contact with the separating
medium. The same applies when removing the separating medium.
Electric shock
WARNING
Defective grounded power outlet, power supply network without
proper grounding, inferior-quality power cord, incorrect line volt-
age, multiple power outlets, extension cords
Risk of electric shock and other injuries to the patient and medical
personnel! Risk of damage to property.
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 Connect the unit / the equipment cart to a properly installed
grounded power outlet.
 Only connect the unit to a power supply network with proper
grounding.
 Only use the Erbe power cord or an equivalent power cord for this
purpose. The power cord must bear the applicable national test
symbol.
 Check the power cord for damage. You must not use a damaged
power cord.
 The supply voltage must match the voltage specified on the unit's
rating plate.
 Do not use multiple power outlets.
 Do not use extension cords.
WARNING
Incorrect line fuse, defective device
Risk of electric shock to the patient and medical personnel! Risk of
damage to property.
 Blown line fuses may only be replaced by a competent technician.
Only replacement fuses that have the same rating as the one
specified on the unit’s rating plate may be used.
 When a fuse has been changed, the function of the unit must be
verified. If the unit does not function properly or if there are any
concerns, please contact Erbe.
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WARNING
Connection of unit / equipment cart and power supply during
cleaning and disinfection
Risk of electric shock to the medical personnel!
 Switch off the device. Unplug the power cord of the device/equip-
ment cart.
Risk of infection
WARNING
Non-sterile applicator connector
The patient can be infected by the use of a non-sterile applicator con-
nector.
 Use aseptic techniques when you connect the applicator connec-
tor with the pump unit for the first time or when replacing the ap-
plicator.
WARNING
A pump unit is used for several patients
Risk of cross-infection.
 A pump unit may only be used for one patient.
WARNING
Non-sterile separating medium
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The patient can be infected by the use of a non-sterile separating

2019-01
medium.
 Only use sterile, physiological saline solutions.
WARNING
Contaminated separating medium
Separating medium splash over the medical staff.
Risk of infection for the medical staff.
 Avoid the accumulation of separating medium in the operating ar-
ea. Ensure adequate suction.
 Use personal protective equipment, e.g. a face mask and splash
guard. The protective equipment must be appropriate for the risk
arising from the patient.
WARNING
Contaminated accessories
 Wear gloves when dismantling the accessories
11 / 62
Fire / explosion
WARNING
Ignition of anesthetics, skin cleansers, and disinfectants in poten-
tially explosive atmospheres
If you place the device in a potentially explosive atmosphere, anes-
thetics, skin cleansers, and disinfectants can ignite.
Risk of fire and explosion to the patient and medical personnel! Risk
of damage to property.
 Do not place the device in potentially explosive atmospheres.
Defective unit, defective accessories
WARNING
Technical safety checks not being done
Risk of injury or death for patients and medical staff! Risk of damage
to property.
 Have the device checked for safety at least once a year.
 You must not use a device that is not safe.
WARNING
Damaged device, damaged accessories, modified device, and
modified accessories
Risk of injury to the patient and medical personnel! Risk of damage
to property.
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 Check the unit and accessories (e.g. footswitch, cables, tubes from
instruments) for damage every time before use.
 You must not use damaged equipment or damaged accessories.
Replace defective accessories.
 If the unit or accessories are damaged, please contact our cus-
tomer service.
 For your safety and that of the patient: Never attempt to perform
repairs or make modifications yourself. Any modification will in-
validate liability on the part of Erbe Elektromedizin GmbH.
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NOTICE
Tension on the suction hose
If you subject the suction hose to tension, secretion can escape from
the branch (1).
 Do not subject the suction hose to tension.
Fig. 1-1
Interference caused by the unit
NOTICE
Use of non-approved internal cables by Technical Service
This can result in the increased emission of electromagnetic waves or
reduce the immunity of the device.
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 Technical Service may only use the internal cables that are listed
in the service manual for the device.
NOTICE
Stacked devices
If you place the device next to or stack it with other equipment, the
devices may affect each other.
The unit may fail or not function properly.
 The unit may only be placed next to or stacked with VIO-series de-
vices.
 If it is necessary to operate the device near or stacked together
with non-VIO-series equipment, keep as much distance as possi-
ble between the devices. Check whether the devices are affecting
each other: Are the devices behaving unusually? Are faults occur-
ring?
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WARNING
Use of non-approved EMC-relevant accessories
This can result in the increased emission of electromagnetic interfer-
ence or reduce the electromagnetic immunity of the device.
Risk of injury to the patient.
 Only use cable that is specified in the table “EMC-relevant acces-
sories,” see chapter “Information on electromagnetic compatibil-
ity (EMC).”
 If you are using accessories from other manufacturers, check
whether the Erbe device is interfering with other devices or being
affected by interference itself. You cannot use the device if there
is any interference.
Safety information for use of ERBEJET 2
WARNING
Unsuitable separating medium
The use of an unsuitable separating medium can change the effect of
the water jet. Risk of injury to the patient.
WARNING
Effect set too high
The higher the effect, the greater the risk of accidental tissue dam-
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age.
 Set effect as low as possible relative to the required surgical ef-
fect.
WARNING
Activation of the unit with no knowledge of active settings
If the user does not understand the active settings of the unit, he can
cause the patient accidental tissue damage.
 Check the active settings on the unit display after setting the unit,
changing a program, or changing a setting.
CAUTION
Uncontrolled water jet
Depending on the effect setting, the water jet can damage skin or the
eyes.
 Never point the water jet at medical personnel. Do not point the
water jet at the patient accidentally.
 Wear goggles for your own safety.
 Point the tip of the applicator at the operating field. Only press the
pedal when you want to cut.
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CAUTION
During the priming process, separating medium can escape from
the applicator.
Depending on the effect setting, the water jet can damage skin or the
eyes.
 Never point the applicator at medical personnel. Never point the
applicator at the patient during the priming process.
 If separating medium escapes from the applicator, stop the prim-
ing process. Press the Selection button next to the menu item.
STOP.
NOTICE
Applicator pressure hose kinked
If you kink the pressure hose you will obtain an error message in crit-
ical cases and have to replace the applicator and pump unit.
 Do not kink the pressure hose.
Notes
Grounding Note: If necessary, the equipment can be connected to the external grounding system
of the room with the grounding pin on the back of the unit and/or Cart using a con-
necting cable designed for this purpose. Affects of low frequency leakage currents due
to a defective grounding system within the room may be eliminated through external
grounding.
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Use of a defibrillator Note: The equipment conforms to the requirements of Type CF and is protected
2019-01
against the effects of a defibrillator discharge.
Membrane keyboards Note: If alcohol-based disinfectants are used on units with membrane keyboards, this
remove the anti-glare finish. However, the user surfaces remain fully functional. This
does not present a hazard.
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2 • Description of the Controls
Chapter 2
Description of the Controls
Controls on the front panel
ERBEJET 2
L1 R1
L2 R2
1
L3 R3
4
2
Fig. 2-1
Symbol (1)
In addition to the user manual, please observe all other documents provided with the
device.
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Power (2) Power switch

Unit on / off. The unit is only fully disconnected from the power supply once the power
cord is pulled out. Install the device such that the power cord could be easily discon-
nected from the power source.
Symbol (3)
The equipment conforms to the requirements of Type CF (Cardiac Float) and is pro-
tected against the effects of a defibrillator discharge.
Pump shaft (4)

Accommodates the pump unit (applied part).
Selection buttons (L1) (L2) (L3) (R1) (R2) (R3)

The buttons have a different function depending on which window is shown on the
display. Take note of the function the button refers to.
17 / 62
2 • Description of the Controls
Controls on the back
6
7
Fig. 2-2
Sockets (1) Footswitch socket

You can connect a single-pedal or a dual-pedal footswitch to this socket.
(2) (3) ECB sockets (ECB means Erbe Communication Bus)
Other compatible units can be connected to ERBEJET 2. The ECB ensures communica-
tion between the units. Connect an ECB cable with these sockets and with one of the
other units.
Potential equalization (4) Potential equalization terminal

Attach a potential equalization line and connect this to the potential equalization sys-
tem of the operating room. If you are using the Erbe VIO-CART, connect the potential
equalization line to the potential equalization pin of the VIO-CART.
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Power fuses (5) Power fuses
The unit is protected with power fuses. If one of these power fuses has blown, the unit
may not be used on the patient again until it has been checked by a competent tech-
nician. The values of the power fuses are specified on the unit's rating plate. Only
spare fuses with these values may be used.
Power connection (6) Power connection

Connect the unit to a properly installed grounded outlet. Only use the Erbe power cord
or an equivalent power cord for this purpose. The power cord must bear the national
test symbol. If the unit is installed on the Erbe VIO-CART, make the power connection
with the power cord of the VIO-CART.
Symbol (7)
Read the user manual before switching on and using the unit.
18 / 62
3 • Working with ERBEJET 2
Chapter 3
Working with ERBEJET 2
Connecting suction module ESM 2, connecting the applicator to the

pump unit, replacing the applicator
If you use an applicator with suction hose you can use the suction module ESM 2 for
suction.
WARNING
to property.
 Check the unit and accessories (e.g. footswitch, cables, tubes
from instruments) for damage every time before use.
tomer service.
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Attaching the mounting bracket
Fig. 3-1
 Equip the bracket with a mounting bracket.
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Hanging the suction container Note: The suction container must be positioned lower than the operating field so that
no fluid can flow back from the suction hose into the operating field.
Fig. 3-2
 Hang the suction container on the mounting bracket.
Inserting the suction bag
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Fig. 3-3
 Insert the suction bag into the suction container.
Connecting ESM 2 with the suction Note: Use a new membrane filter in the following cases:
container • For each new application (new operation).
• If the membrane filter has been unpacked for longer than 7 days.
• If the membrane filter has absorbed moisture.
Fig. 3-4
1. Connect the vacuum hose with the membrane filter.
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Fig. 3-5
2. Use the vacuum hose to connect the ESM 2 to the suction container directly. Plug
the membrane filter onto the ESM 2.
Connecting the applicator to the

pump unit, replacing the applicator WARNING
A pump unit is used for several patients
Risk of cross-infection.
 A pump unit may only be used for one patient.
WARNING
Non-sterile applicator connector
The patient can be infected by the use of a non-sterile applicator
connector.
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 Use aseptic techniques when you connect the applicator connec-

tor with the pump unit for the first time or when replacing the
applicator.
Fig. 3-6
 Connect the applicator connector with the pump unit. The applicator connector
must audibly click into place.
21 / 62
Fig. 3-7
The pump unit is intended for the treatment of one patient. The applicators can be re-
placed any number of times during the treatment of this one patient.
 Press the release mechanism (1) to release the applicator.
Selecting program, Inserting pump unit, Connecting separating

medium, Priming pump unit and applicator
Selecting a program
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L1 R1
L2 R2
L3 R3
Fig. 3-8
1. Use the power switch to switch the unit on. The unit carries out a performance
test. The connected units and footswitches are recognized. The version number of
the software appears on the display.
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L1 R1
L2 R2
L3 R3
Fig. 3-9
2. You will then see a selection list of programs.

3. Select a program with the selection buttons R1, R3. Example setting: BASIC PRO-
GRAM.
4. Confirm your selection. Press the selection button next to the menu item OK.
Inserting the pump unit into

ERBEJET 2
L1 R1
L2 R2
L3 R3
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Fig. 3-10
You come to the Settings window. The ERBEJET prompts you to insert a new pump.
Fig. 3-11
1. Slide the pump unit into the pump shaft. The pump unit must audibly click into place.
23 / 62
L1 R1
L2 R2
L3 R3
Fig. 3-12
2. As soon as the pump unit has been connected, the ERBEJET prompts you to prime
the pump unit and applicator with separating medium.
Connecting the separating medium

WARNING
Unsuitable separating medium
The use of an unsuitable separating medium can change the effect
of the water jet. Risk of injury to the patient.
WARNING
Non-sterile separating medium
The patient can be infected by the use of a non-sterile separating
medium.
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1. Allow the separating medium to run to the end of the infusion tube.
Fig. 3-13
2. Remove the protective cap from the pump unit. Connect the infusion tube to the
Luer-Lock adapter (1) on the pump unit.
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Priming the pump unit and

applicator
L1 R1
L2 R2
L3 R3
Fig. 3-14
L1 R1
L2 R2
L3 R3
Fig. 3-15
CAUTION
During the priming process, separating medium can escape from
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the applicator.
Depending on the effect setting, the water jet can damage skin or
the eyes.
 Never point the applicator at medical personnel. Never point the
applicator at the patient during the priming process.
 If separating medium escapes from the applicator, stop the
priming process. Press the Selection button next to the menu
item. STOP.
1. Prime the pump unit and applicator with separating medium. Press the Selection
button next to the menu item. START. If you press the Selection button next to the
menu item SKIP, you skip over the priming process. You must then prime the
pump unit and applicator with separating medium by activating the water jet.
2. The menu item STOP must be activated if separating medium escapes from the
applicator during the priming process (see Safety instructions). If you activate the
menu item STOP before the priming process is completed, you must prime the
pump unit and applicator with separating medium by activating the water jet.
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Mounting suction hose of applicator to suction container
NOTICE
Tension on the suction hose
If you subject the suction hose to tension, secretion can escape
from the branch (1).
 Do not subject the suction hose to tension.
Fig. 3-16
Note: The ESM 2 may be operated only in combination with a suction hose that is in-
tegrated in an applicator of the ERBEJET 2.
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Fig. 3-17
1. Attach the adapter to the connection for the suction hose.
Fig. 3-18
2. Attach the suction hose to the adapter.
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Window settings, Selecting effect, Setting suction
Window settings
3
4
L1 R1
2
L2 R2
1
L3 R3
Fig. 3-19
The following parameters are stored in each program:

• Effect
• Settings for Suction
In the window Settings you can:
• Select Effect (1).
• Change to the Suction (2) window.
• Change to the Program / Setup (3) window.
• Eject the pump unit by pressing the selection button R1. Activate the menu item
EJECT (4).
Selecting effect
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L1 R1
L2 R2
L3 R3
Fig. 3-20
Select an Effect with the selection buttons R2, R3. Example setting: Effect 45.
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Setting suction
L1 R1
L2 R2
L3 R3
Fig. 3-21
If ERBEJET 2 is connected to an ESM 2 suction module, you can also apply suction with
a suitable applicator, as well as cut.
Press the selection button next to the menu item Suction.
L1 R1
L2 R2
L3 R3
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Fig. 3-22
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You can perform several settings in the Suction window:
1. Suction mode
Press the selection button R3 to set the suction mode.
• Off: Suction is off.
• Cont: Suction works continuously, independent of activation of ERBEJET 2.
• Pedal: Suction works with pedal activation. In the example display, this setting is
active. You will find details on activation of suction and the water jet under the
heading Activation.
2. Vacuum for suction
Select the vacuum for Suction with the selection buttons R1, R2. The vacuum can be
selected in the range -100 to -800 mbar. Example setting: -400 mbar.
3. Run-on time
After the water jet activation is finished, suction continues for the set run-on time.
Press the selection button L3 to set the Run-on time.
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L1 R1
L2 R2
L3 R3
Fig. 3-23
Select a run-on time in the range 1 to 60 sec. with the selection buttons R1, R2. Ex-
ample setting: 60 sec.
The run-on time can also be switched off: Setting OFF.
Press the selection button next to the menu item Return.
Activation
WARNING
Contaminated separating medium
Separating medium splash over the medical staff.
 Avoid the accumulation of separating medium in the operating
area. Ensure adequate suction.
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 Use personal protective equipment, e.g. a face mask and splash

guard. The protective equipment must be appropriate for the risk
arising from the patient.
Activating with the single-pedal

footswitch What do you want to Setting in the Suction Activating the
activate? menu (GB) pedal
only water jet Off yes
continuous suction independent Cont. no

of activation of ERBEJET 2
water jet + suction independent Cont. yes

of activation of ERBEJET 2
water jet + suction Setting pedal + run-on yes

time off
water jet + suction + run-on Setting pedal + run-on yes

time for suction time 1- 60 sec.
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Activating with the dual-pedal

footswitch What do you want to activate? Setting in the Suction Activating
menu (GB) pedal
only water jet Off right-hand pedal
only suction independent of acti- Cont. none

vation of ERBEJET 2
only suction pedal left-hand pedal
water jet + suction independent of Cont. right-hand pedal

activation of ERBEJET 2
water jet + suction Setting pedal + run-on right-hand pedal

time off
water jet + suction + run-on time Setting pedal + run-on right-hand pedal
for suction time 1- 60 sec.
Note: When activating ERBEJET 2, the set effect is shown inverted on the display
(white numbers on blue background).
Note: During suction, the set maximum vacuum is shown inverted on the display of
ERBEJET 2 (white numbers on blue background).
Saving a modified basic program as a new program, Selecting program,

Saving programs for the ReMode function
Saving a modified basic program as

a new program
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L1 R1
L2 R2
L3 R3
Fig. 3-24
In the preceding stages of the tutorial you made changes to the settings of the basic
program. The modified basic program is marked with a * in the display.
The settings will be lost if they are not saved. You cannot overwrite the basic program
with your settings. The basic program cannot be changed. However, you can save
changed settings of the basic program as a new program.
All settings will then be stored as a complete setting in the memory.
1. Press the selection button next to the menu item Program / Setup.
2. Press the selection button next to the menu item SAVE / ERASE program.
3. Press the selection button next to the menu item SAVE.
4. Press the selection button next to the menu item SAVE settings as new program.
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L1 R1
L2 R2
L3 R3
Fig. 3-25
5. Select a number (a memory location) for the program with the selection buttons
R2, R3. Example: 1
6. Press the selection button next to the menu item NAME / SAVE.
L1 R1
L2 R2
L3 R3
Fig. 3-26
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7. Select a letter or a number with the selection buttons R1, R3.

2019-01
8. Move the character one place to the right with the selection button L2.
9. Select the next character. Example: TEST.
10. Press the selection button next to the SAVE menu item until the message PRO-
GRAM SAVED appears.
11. Press the selection button next to the Return symbol.
Selecting a program 1. Press the selection button next to the menu item Program / Setup.
2. Press the selection button next to the menu item SELECT program.
L1 R1
L2 R2
L3 R3
Fig. 3-27
3. Select a program with the selection buttons R1, R3. Example: BASIC PROGRAM.
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Saving programs for the ReMode With the footswitch ReMode switch you can change between two program levels a and
function b of a program. You have to save a program with two program levels a and b for this
purpose.
Creating and saving program a
L1 R1
L2 R2
L3 R3
Fig. 3-28
1. Create a program by changing the settings of the BASIC PROGRAM.

2. Save the modified basic program at memory location 2 with the name EXAMPLE.
You can also take any other name and any other memory location.
The identifier a is automatically assigned to the program after program b is created.
Creating and saving program b
L1 R1
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L2 R2
L3 R3
Fig. 3-29
1. Change the settings of program 2 EXAMPLE.

5. Press the selection button next to the menu item SAVE settings as new program.
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L1 R1
L2 R2
L3 R3
Fig. 3-30
6. The window automatically offers you the number 2 b. Press the selection button
next to the menu item NAME / SAVE.
GRAM SAVED appears.
8. Press the selection button next to the menu item Return.
In the Settings window you see the program 2 b EXAMPLE.
Call up the window Select program . You will then see in a selection list of programs
that the program 2 EXAMPLE has been renamed as 2 a EXAMPLE.
With the footswitch ReMode switch you can change between the two program levels
a and b of the program 2 EXAMPLE if you have selected the program level 2 a EXAM-
PLE or 2 b EXAMPLE.
Deleting a program, Overwriting a program

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Deleting a program 1. Press the selection button next to the menu item Program / Setup.
3. Press the selection button next to the menu item ERASE program.
4. Press the selection button next to the ERASE program menu item until the mes-
sage PROGRAM ERASED appears.
Overwriting a program 1. Press the selection button next to the menu item Program / Setup.
4. Press the selection button next to the menu item OVERWRITE current program.
GRAM SAVED appears.
ml-Signal
You can turn on the ml-Signal in Setup of ERBEJET 2 (see also Setup). A tone sounds
after the emission of every ml separating medium.
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Displaying used separating medium, Resetting display
Displaying used separating

medium
L1 R1
L2 R2
L3 R3
Fig. 3-31
If in the Service Setup menu the option Volume Measurement is turned on, you can
display the amount of used separating medium. To activate this option, contact an
Erbe representative.
L1 R1
L2 R2
L3 R3
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Fig. 3-32
2. Press the Selection button next to the menu item. Info.
L1 R1
L2 R2
L3 R3
Fig. 3-33
Resetting display When inserting a new pump unit, the display of the liquid volume is automatically reset
to 0. You can also manually reset the display of the liquid volume to 0. This is possible
with every pump unit as often as one likes.
Press the Selection button next to the menu item. Reset.
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Having the unit of pressure set

In the Service Setup menu under the menu item Unit of pressure, you can have the
units mbar, psi or kPa set.
When you have the unit psi set, the effect (when set) is converted to psi. Under the
Effect Display, the corresponding psi value temporarily appears.
Accessing Setup
In Setup you can, for example, adjust the unit to the light conditions in the room.
2. Press the selection button next to the menu item SETUP.
L1 R1
L2 R2
L3 R3
Fig. 3-34
3. Select a Setup setting with the selection buttons L1, L3. Example: Contrast.
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L1 R1
L2 R2
L3 R3
Fig. 3-35
5. Select a setting with the selection buttons R2, R3. Example: Contrast 5.
6. Confirm your selection. Press the selection button next to the menu item Return.
You can perform the following settings:
• Contrast: Contrast in 10 levels.
• Display brightness: Brightness in 10 levels.
• Volume of button sound: Volume of button sound in 10 levels.
• Volume of ml-Signal: Volume of the ml-Signal in 10 levels. When you turn on the
ml-Signal, a tone sounds after the emission of every ml separating medium.
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• Volume of alarm sound: Volume of the warning signals in 8 levels. The warning
signals must be clearly audible!
• Volume of activation sound: Volume of the activation sound in 10 levels. The
activation sound must be clearly audible!
• Automatic time: Display duration of the window on the display from 3-30 sec-
onds. If you select the Off setting, the corresponding window remains displayed
for an unlimited time.
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4 • Status Messages, Error Messages
Chapter 4
Status Messages, Error Messages
Status messages
Status messages are of an informative nature or prompt you to take operational ac-
tion.
Status message Description
Suction Module recognized! You have switched on the ESM 2 suction module at the power switch or have
connected with the ECB cable.
Ready The pump unit is connected. ERBEJET 2 is ready for activation.
The footswitch is ready for operation. You have connected the footswitch.
The footswitch has been disconnected. You have removed the footswitch.
ERBEJET has cooled down. / Activation is ERBEJET 2 has cooled down sufficiently after overheating so that activation is
possible again! possible again.
Press "START" to prime. Press the Selection button next to the menu item START to prime the pump
unit with separating medium.
Priming running Priming running

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Priming completed. Priming completed.
Priming aborted You have aborted the priming by pressing the STOP button.
Remove used cartridge! Remove the pump unit from the pump shaft.
Please insert new cartridge! Slide the unused pump unit into the pump shaft.
Connecting cartridge - Please wait. Wait until the pump unit is disconnected.
Uncoupling cartridge - Please wait. Wait until the pump unit is unlocked.
Referencing running - Please wait. The pump unit drive can be in various positions after switching on ERBEJET 2.
The drives therefore start by moving right to the back (reference position).
Referencing completed. The pump unit drives have reached the reference position.
Error messages
An error message consists of an error code (EC.) and an error text. The ERBEJET 2 dis-
play shows two different types of error messages.
a) Error messages that prompt you to take action and remedy the error. You will find
these error messages in the table.
b) Error messages that prompt you to inform Technical Service. These error messages
are not described individually in the user manual. The error text reads:
• Please inform Technical Service.
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Please note the error code. Give the error code to Technical Service.
You will find error messages with error code outputs in numerical order.
Error messages with error codes in numerical order
EC. Error text Possible cause(s) What should you do?
J-5D ESM 2: Software incompati- The ESM 2 suction module has non-com- Use an ESM 2 suction module with
ble! patible software. compatible software. Inform Techni-
cal Service.
J-5E FS: Software incompatible! The footswitch has incompatible software. Use a footswitch with compatible
software. Inform Technical Service.
J-06 Activation has been inter- System error Reactivate ERBEJET 2. If the error
rupted. occurs frequently, inform Technical
Service.
J-07 Please check the position of The pump unit may have been pushed out If the pump unit is not correctly
the cartridge in the slot! of the pump shaft. seated in the pump shaft, firstly
attempt to press the pump unit back
in place. The error message disap-
pears if successful. If this action
fails, press the selection button next
to the EJECT display. Remove the
pump unit and applicator. Take a new
pump unit and a new applicator. If
the error occurs frequently, inform
Technical Service.
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J-20 Module conn. to ECB not A non-compatible device is connected to the Remove the device by detaching the
2019-01
compatible. ECB socket of ERBEJET 2. ECB cable between the device and
ERBEJET 2.
J-21 Check date/clock time The battery is discharged. Date and time You can still work with ERBEJET 2,
adjustment. may have been lost. but inform Technical Service none-
theless.
J-23 Check date/clock time Date and time are inconsistent. You can still work with ERBEJET 2,
adjustment. but inform Technical Service none-
theless.
J-24 Module conn. to ECB not A non-compatible footswitch is connected Remove the footswitch.
compatible. to ERBEJET 2.
Error messages
Error text Possible cause(s) What should you do?
Suction: activation inter- System error Reactivate the ESM 2 suction module. If
rupted. the error occurs frequently, inform Tech-
nical Service.
Suction OFF You have attempted to activate the ESM 2 suction Set the suction mode to PEDAL.
module, but the suction is deactivated in the Suc-
tion window of the ERBEJET 2 display. Suction
mode: OFF
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Suction not ready for oper- Various causes are possible:

ation!
a) The ESM 2 suction module is not connected. a) Switch on the ESM 2 suction module
with the power switch.
b) There is no connection between ERBEJET 2 b) Check the connection between ERBE-

and the ESM 2 suction module. JET 2 and the ESM 2 suction module
(ECB cable).
c) System error.
c) Inform Technical Service.
Please interrupt activation. a) You keep the pedal depressed. a) Release the pedal.
b) System error b) Inform Technical Service.
ERBEJET 2 not ready for a) You have attempted to activate ERBEJET 2 a) Do not activate until the following
operation! before the pump unit drives were ready. message is displayed: "Ready."
b) You have attempted to activate ERBEJET 2 b) Insert a pump unit.

without a pump unit.
ERBEJET overheated / The temperature of the pump unit drives is too Let ERBEJET 2 cool down until the fol-
Activation not possible! high. The drives have been switched off. lowing message is displayed:
"ERBEJET has cooled down! / Activation

is possible again!"
Error: Powerfail System error Reactivate ERBEJET 2. If the error occurs

frequently, inform Technical Service.
The footswitch is not ready. Various causes are possible:

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a) No footswitch is connected. a) Connect a footswitch to ERBEJET 2.
b) The footswitch has incompatible software. b) Use a footswitch with compatible soft-
ware.
c) Inform Technical Service.
You have exceeded the ON time limit attained. Options:

max. ON time!
a) Observe the max ON time.
b) Extend the max ON time.
c) Switch off the ON time limit.
ReMode: Level 'b' is not You have pressed the ReMode button on the a) Do not press the ReMode button.
available! footswitch, but have not selected a program with
two program levels. Only a program with two b) Select a program with two program
program levels can be activated with the ReMode levels.
button.
Critical temperature The temperature of the pump unit drives is high. If possible, take activation breaks. Check
reached! / Let ERBEJET ERBEJET 2 is ready for reactivation. whether air can freely circulate around
cool down! the ERBEJET 2 housing.
Program not documented. You are trying to delete a program that is not Try not to delete any undocumented pro-
documented. grams.
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Pulsemode is not available! The pulse mode is a software option and is not You have pressed the selection button
available in the device or is not yet released. next to the place holder for the pulse
mode option.
Instrument damaged or Various causes are possible: Press the selection button next to the
pump reused. Replace EJECT display. Remove the pump unit
pump and instrument. a) The applicator nozzle is clogged. and applicator. Take a new pump unit and
a new applicator. If the action fails,
b) You are attempting to connect a used pump inform Technical Service.
unit to the drive.
c) The drive is blocked or too stiff.
d) The drive mechanism is defective.
Keyboard error Various causes are possible:
a) You pressed a button when starting. a) Restart ERBEJET 2 without pressing a

button.
b) Button jammed. b) Inform Technical Service.
Two switches simultane- You have pressed both footswitch pedals at the Press just one pedal.
ously. same time.
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5 • Installation
Chapter 5
Installation
Ambient conditions
WARNING
Ignition of anesthetics, skin cleansers, and disinfectants in poten-
tially explosive atmospheres
If you place the device in a potentially explosive atmosphere, anes-
thetics, skin cleansers, and disinfectants can ignite.
Risk of fire and explosion to the patient and medical personnel! Risk
of damage to property.
 Do not place the device in potentially explosive atmospheres.
NOTICE
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NOTICE
Unsuitable temperature or level of humidity during operation
If you operate the equipment at an unsuitable temperature or level of
humidity, it may sustain damage, fail, or not perform properly.
 Operate the equipment at a suitable temperature and level of hu-
midity. You will find the tolerances for temperature and humidity
in the Technical Data.
 If other ambient conditions must be observed for operation of the
equipment, you will also find them in the Technical Data.
NOTICE
Unsuitable temperature or humidity in transit or storage
If you transport or store the equipment at an unsuitable temperature
or level of humidity, it may sustain damage and fail.
 Transport and store the equipment at a suitable temperature and
level of humidity. You will find the tolerances for temperature and
humidity in the Technical Data.
 If other ambient conditions must be observed for transport and
storage of the equipment, you will also find them in the Technical
Data.
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5 • Installation
NOTICE
Insufficient acclimatization time, unsuitable temperature during
acclimatization
If the device was stored or transported below or above a certain tem-
perature, it will take a certain time and temperature to acclimatize.
If you do not observe the rules, the device can sustain damage and
fail.
 Acclimatize the device according to the rules in the Technical Da-
ta.
NOTICE
Overheating of the device due to poor ventilation
If ventilation is poor, the device can overheat, sustain damage, and
fail.
 Install the device in such a way that there is an unobstructed cir-
culation of air around the housing. Installation in confined wall re-
cesses is prohibited.
NOTICE
 Take care when connecting the separating medium to the pump
unit that the unit does not come into contact with the separating
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medium. The same applies when removing the separating medi-
2019-01
um.
WARNING
to property.
tomer service.
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5 • Installation
Electrical installation
WARNING
Defective grounded power outlet, power supply network without
proper grounding, inferior-quality power cord, incorrect line volt-
age, multiple power outlets, extension cords
Risk of electric shock and other injuries to the patient and medical
personnel! Risk of damage to property.
 Connect the unit / the equipment cart to a properly installed
grounded power outlet.
 Only connect the unit to a power supply network with proper
grounding.
 Only use the Erbe power cord or an equivalent power cord for this
purpose. The power cord must bear the applicable national test
symbol.
 Check the power cord for damage. You must not use a damaged
power cord.
 The supply voltage must match the voltage specified on the unit's
rating plate.
 Do not use multiple power outlets.
 Do not use extension cords.
WARNING
Incorrect line fuse, defective device
Risk of electric shock to the patient and medical personnel! Risk of
damage to property.
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 Blown line fuses may only be replaced by a competent technician.

2019-01
Only replacement fuses that have the same rating as the one
specified on the unit’s rating plate may be used.
 When a fuse has been changed, the function of the unit must be
verified. If the unit does not function properly or if there are any
concerns, please contact Erbe.
WARNING
to property.
tomer service.
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5 • Installation
Installing ERBEJET 2
• To ensure the unit stands safely and free of vibration, place it on a stable, hori-
zontal, vibration-free surface.
• Avoid direct sunlight for reasons of heating and good display legibility.
• Turn the rear of the unit away from the operating field.
• Lock the wheel brakes on the front wheels.
• The supply voltage must match the voltage specified on the unit's rating plate.
• Connect the unit to a properly installed grounded outlet. Only use the Erbe power
cord or an equivalent power cord for this purpose. The power cord must bear the
national test symbol. If the unit is installed on the VIO-CART, make the power con-
nection with the power cord of the VIO-CART.
• Install the device such that the power cord could be easily disconnected from the
power source.
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6 • Disassembly, Cleaning and Disinfection
Chapter 6
Disassembly, Cleaning and Disinfection
Removal of separating medium; disassembly of ESM 2 suction unit,

applicator, and pump unit
WARNING
Contaminated accessories
 Wear gloves when dismantling the accessories
Removing separating medium Remove the separating medium from the pump unit. Dispose of the separating medi-
um.
Detaching the suction hose from 1. Disconnect the suction hose of the applicator from the suction bag (no picture).
the suction bag
II.
I.
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Fig. 6-1
2. Remove the adapter and attach the adapter to the plug and connector on the top
(I.) intended for this purpose.
3. Use the cap (II.) to close the connection for the suction hose.
Removing the suction bag
Fig. 6-2
 Remove the suction bag from the suction container and dispose of the suction bag
in a suitable way.
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Removing the pump unit with

applicator
L1 R1
L2 R2
L3 R3
Fig. 6-3
 Press the selection button next to the menu item EJECT. The pump unit unlocks.
Observe the instructions on the display. Remove the pump unit. Dispose of the
pump unit and applicator.
Detaching the vacuum hose from Note: The vacuum hose can remain attached to the suction container for the next ap-
ESM 2 plication.
1. Disconnect the vacuum hose (together with the membrane filter) from the ESM 2.
2. Separate the membrane filter from the vacuum hose and dispose of the mem-
brane filter is a suitable way.
Dismantling the suction container If you want to undertake cleaning going beyond wipe disinfection:
and mounting bracket
1. Separate the vacuum hose from the suction container and pull the suction con-
tainer out of the mounting bracket.
2. Remove the mounting bracket from the bracket.
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Wipe disinfection
For cleaning and disinfecting the surfaces of the unit or of the equipment cart, Erbe
recommends a wipe disinfection. Use only disinfectant which complies with the rele-
vant national standards.
WARNING
Connection of unit / equipment cart and power supply during
cleaning and disinfection
Risk of electric shock to the medical personnel!
 Switch off the device. Unplug the power cord of the device/equip-
ment cart.
NOTICE
46 / 62
NOTICE
Alcohol-based spray disinfectant for fast disinfection
With membrane keyboards and paint surfaces there is the risk of
cracks. Propanol and ethanol will erode surfaces.
 Do not use these substances.
NOTICE
Alternate use of disinfectant solutions based on different active
ingredients
A color reaction may occur with plastics.
 Do not use these substances alternately.
Instructions for cleaning and disinfection

Mix the disinfectant in the concentration specified by the manufacturer.
Clean surfaces contaminated with blood before using the disinfectant; otherwise it
may be less effective.
Wipe the surfaces. Make sure the surfaces are treated uniformly. Comply with the ac-
tion time of the disinfectant specified by the manufacturer.
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7 • Technical Data
Chapter 7
Technical Data
Power connection
Rated supply voltage 100 – 240 V
Line current 0.4 – 1.2 A
Rated supply frequency 50 Hz / 60 Hz
Power fuses 2 x T 3.15 A H / 250 V
Data specific to the unit
Pressure production Sterile single-use double cylinder pump
Pressure range in bar 1 – 80 (± 20 %)
Volume flow in ml/min. 1 – 55 (± 10 %)
Effect setting Setting of indication-specific parameters with 9 program

memory locations
Activation Footswitch
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Separating medium Sterile, physiological saline solutions
Suction as a separate module (Erbe ESM 2) adjustable -100 to -800 mbar (± 50 mbar)
Applicators Sterile single-use applicators, rigid and flexible for open, lap-
aroscopic, endoscopic, microsurgical, minimal-invasive and
micro-invasive applications, from 1.3 mm outer diameter.
Nozzle diameter 120 μm
Dimensions and weight
Width x height x depth 410 x 130 x 370 mm
Weight 11 kg
Ambient conditions for transport and storage of unit
Temperature -25 °C to +50 °C
Relative humidity 15 % – 80 %
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7 • Technical Data
Ambient conditions for operation of the unit
Temperature +10 °C to +40 °C
Relative humidity 15% – 80%, noncondensing
Acclimatizing
If the unit has been stored or transported at temperatures below +10 °C or above +40 °C, the unit will require approx. 3 hours
to acclimatize at room temperature.
Standards
Classification according to EC Directive 93/42/EEC II b
Protection class as per EN 60 601-1 I
Type as per EN 60 601-1 CF
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8 • Information on electromagnetic compatibility (EMC)
Chapter 8
Information on electromagnetic
compatibility (EMC)
Where EMC is concerned, medical electrical equipment is subject to special safety

measures and must be installed and commissioned according to the EMC instructions
stated herein.
WARNING
Use of non-approved EMC-relevant accessories
This can result in the increased emission of electromagnetic interfer-
ence or reduce the electromagnetic immunity of the device.
Risk of injury to the patient.
 Only use cable that is specified in the table “EMC-relevant acces-
sories,” see chapter “Information on electromagnetic compatibil-
ity (EMC).”
 If you are using accessories from other manufacturers, check
whether the Erbe device is interfering with other devices or being
affected by interference itself. You cannot use the device if there
is any interference.
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NOTICE
Stacked devices
If you place the device next to or stack it with other equipment, the
devices may affect each other.
 The unit may only be placed next to or stacked with VIO-series de-
vices.
 If it is necessary to operate the device near or stacked together
with non-VIO-series equipment, keep as much distance as possi-
ble between the devices. Check whether the devices are affecting
each other: Are the devices behaving unusually? Are faults occur-
ring?
NOTICE
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NOTICE
Use of non-approved internal cables by Technical Service
This can result in the increased emission of electromagnetic waves or
reduce the immunity of the device.
 Technical Service may only use the internal cables that are listed
in the service manual for the device.
Guidance and manufacturer's declaration - electromagnetic emissions
The equipment is intended for use in the electromagnetic environment specified below. The customer or the user of the
equipment should ensure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
HF emissions CISPR 11 Group 1 The device only uses HF energy for its internal func-
tion.
HF emissions CISPR 11 Class A The properties of this device in terms of its emissions
mean it can only be used in hospitals that are con-
Harmonic emissions IEC 61000-3-2 Class A nected to supply systems specifically provided for that
Voltage fluctuations/flicker emissions Complies purpose (usually supplied via isolating transformers).
IEC 61000-3-3 For domestic use (for which class B is usually required
as per CISPR 11), this device may not offer adequate
protection against radio services. The user may need
to take corrective measures such as relocating or
reorienting the device.
Guidance and manufacturer's declaration - electromagnetic immunity
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The equipment is intended for use in the electromagnetic environment specified below. The customer or the user of the
equipment should ensure that it is used in such an environment.
Immunity test IEC 60601-1-2 test level Compliance level Electromagnetic environment
- guidance
Discharge of static ±8 kV contact discharge ±8 kV contact discharge The floor should be made from
electricity (ESD) in wood or concrete or be covered
accordance with ±15 kV air discharge ±15 kV air discharge with ceramic tiles. If the floor is
IEC 61000-4-2 covered with non-conductive
synthetic material, the relative
humidity must be at least 30%.
Electrical fast tran- ±2 kV for power supply lines ±2 kV for power supply lines Mains power quality should be
sient/burst IEC 61000- that of a typical commercial or
4-4 ±1 kV for input/output lines ±1 kV for input/output lines hospital environment.
Surge IEC 61000-4-5 ±1 kV differential mode ±1 kV differential mode Mains power quality should be
that of a typical commercial or
±2 kV common mode ±2 kV common mode hospital environment.
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Voltage dips, short- 0% UT for 0.5 cycle, 0% UT for 0.5 cycle, Mains power quality should be
term interruptions and at 0, 45, 90, 135, 180, 225, at 0, 45, 90, 135, 180, 225, that of a typical commercial or
voltage fluctuations on 270 and 315 degrees 270 and 315 degrees hospital environment.
power supply input
lines as per 0% UT for 1 cycle, 0% UT for 1 cycle, If the user of the equipment
IEC 61000-4-11 single-phase at 0 degrees single-phase at 0 degrees requires continued operation
during power mains interrup-
70% UT for 25/30 cycles, 70% UT for 25/30 cycles, tions, it is recommended that
single-phase at 0 degrees single-phase at 0 degrees the equipment be powered
Voltage monitoring as 0% UT for 250/300 cycles 0% UT for 250/300 cycles from an uninterruptible power
per IEC 61000-4-11 (50/60 Hz) (50/60 Hz) supply or a battery.
Power frequency (50/ 30 A/m 30 A/m Power frequency magnetic

60 Hz) magnetic field fields should be at levels char-
as per IEC 61000-4-8 acteristic of a typical location in
a typical commercial or hospital
environment.
Note: UT is the a.c. mains voltage prior to application of the test level.
The equipment is intended for use in the electromagnetic environment specified below. The user of the equipment should
ensure that it is used in such an environment.
Immunity test IEC 60601-1-2 test Compliance level Electromagnetic environment - guidance
level
Conducted HF distur- 3 Veff 3 Veff The field strengths of fixed transmitters, as deter-
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2019-01
IEC 61000-4-6 below the compliance level in each frequency

6 Veffa) in ISM fre- 6 Veffa) in ISM fre- range. b)
quency bands quency bands
150 kHz to 80 MHz 150 kHz to 80 MHz Interference may occur in the vicinity of equipment
marked with the following symbol.
Radiated high-fre- 3 V/m 3 V/m
quency electromag- 80 MHz to 2.7 GHz 80 MHz to 2.7 GHz
netic fields as per
IEC 61000-4-3
Note: These guidelines may not apply in all cases. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
a)
The ISM bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz, 13.553 MHz to 13.567 MHz, 26.957 MHz to
27.283 MHz and 40.66 MHz to 40.7 MHz.
b)
The field strengths of fixed transmitters, such as base stations for radio (cellular/cordless) telephones and terrestrial radio
equipment, amateur radio stations, AM and FM radio and TV channels cannot be predicted theoretically with accuracy. To
assess the electromagnetic environment with regard to fixed transmitters, a site inspection should be considered. If the field
strength measured at the site where the device is used exceeds the abovementioned compliance level, the device must be
monitored to ensure it is functioning properly. In the event of any unusual operating behavior, additional measures may be
required, such as changing the orientation or location of the device.
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Electromagnetic immunity against high-frequency wireless communication devices as per IEC 61000-4-3
Frequency band (MHz) Test frequency (MHz) Modulation Compliance level (V/m)
380 - 390 385 Pulse a) (18 Hz) 27
430 - 470 450 FM ± 5 kHz deviation or 28

pulse a) (18 Hz)
704 - 778 710, 745, 780 Pulse a) (217 Hz) 9

a)
800 - 960 810, 870, 930 Pulse (18 Hz) 28
1700 - 1990 1720, 1845, 1970 Pulse a) (217 Hz) 28
2400 - 2570 2450 Pulse a) (217 Hz) 28
5100 - 5800 5240, 5500, 5785 Pulse a) (217 Hz) 9
Note: A minimum safety distance of 30 cm should be maintained between the device and portable HF telecommunications
equipment that transmits in the stated frequency band. This includes mobile phones, WLAN and RFID, and Bluetooth devices.
Failure to comply may lead to a reduction in the device’s performance features.
Interference may occur in the vicinity of equipment marked with the following symbol.
a) The pulse modulation is defined as a square-wave signal with a 50% duty factor.
The cables/cords used on the device must not exceed the lengths specified below.
EMC-relevant accessories a)
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Name Maximum cable length
Power cord 5m
Grounding cable (POAG) 10 m
Footswitch cable 5m
a) EMC-relevant accessories refers to the cable specified. The cable can affect the device’s electromagnetic interference or
the electromagnetic immunity of the device.
Operating environment
For the intended use, the unit may only be operated in premises used for medical pur-
poses.
The device may be operated in the vicinity of an electrosurgical unit. The safety in-
structions for the device and the electrosurgical unit must be observed. Please read
the safety instructions on the following subjects in particular:
• distance between the device and the electrosurgical unit. In this user manual,
refer to the safety instruction Stacked devices.
• Distances between the device and the electrosurgical unit’s cords.
• Distances between the device's cords and the electrosurgical unit’s cords.
Position the devices and cords so that they are as far apart as possible.
Essential performance features
The device does not have any essential performance features within the meaning of
IEC 60601-1.
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9 • Maintenance, Customer Service, Warranty, Disposal
Chapter 9
Maintenance, Customer Service, Warranty,
Disposal
Maintenance
Modifications and repairs Modifications and repairs must not impair the safety of the equipment or equipment
cart and accessories for the patient, user and the environment. This condition is met
when changes to the structural and functional characteristics are not detrimental to
safety.
Authorized persons Modifications and repairs may only be undertaken by Erbe or by persons expressly au-
thorized by Erbe. Erbe accepts no liability if modifications and repairs to the unit or
accessories are made by unauthorized persons. This will also invalidate the warranty.
Technical safety checks The technical safety checks determine whether the safety and operational readiness
of the unit or the equipment cart and accessories conform to a defined technical re-
quired status. Technical safety checks must be performed at least once a year.
What technical safety checks must For this device the following technical safety checks have been stipulated:
be performed?
• Checking of labels and User Manual
• Visual inspection of unit and accessories for damage
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• Testing the grounded conductor in accordance with IEC 60601-1 Section 18

• Testing the leakage current in accordance with IEC 60601-1 Section 19
• Functional testing of all the unit's operating and control elements
• Testing the monitoring equipment
• Testing of mechanical pressure production
The results of the safety checks must be documented.
If during the safety checks any defects are found which might endanger patients, staff
or third parties, the device may not be operated until the defects have been remedied
by competent service technicians.
Customer service
If you are interested in a maintenance contract, please contact Erbe Elektromedizin in
Germany, or your local contact in other countries. This may be an Erbe subsidiary, an
Erbe representative or a distributor.
Warranty
The General Terms and Conditions or the conditions of the purchase contract apply.
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9 • Maintenance, Customer Service, Warranty, Disposal
Disposal
Your product bears a crossed-out garbage can icon (see image). Meaning: In all EU
countries this product must be disposed of separately in accordance with the national
laws implementing EU Directive 2002/96/EC of January 27, 2003, WEEE.
In non-EU countries the local regulations must be observed.
If you have any questions about disposal of the product, please contact Erbe Elektro-
medizin or your local distributor.
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10 • Combination with other equipment, Third-party accessories
Chapter 10
Combination with other equipment,
Third-party accessories
You can connect ERBEJET 2 with the Erbe ESM 2 suction module via an ECB cable. The
functions of the ESM 2 suction module are then shown on the ERBEJET 2 display. You
obtain a mutually communicating system.
You cannot connect suction systems from other manufacturers via an ECB cable to ER-
BEJET 2.
You can connect the suction hose from Erbe applicators for ERBEJET 2 with suction
systems from other manufacturers. The vacuum of the suction system must not ex-
ceed -800 mbar.
You cannot use applicators from other manufacturers with ERBEJET 2.
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10 • Combination with other equipment, Third-party accessories
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11 • Accessories
Chapter 11
Accessories
Introduction
The following offers an overview of example accessories for each accessory category.
A complete overview is available in the Erbe accessories catalog and on the Erbe web-
site. We recommend the use of Erbe accessories.
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11 • Accessories
ERBEJET 2 example accessories
HybridKnife Accessories for ERBEJET 2
Applicators and probes
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ESM 2 (suction module for liquids) Equipment cart and accessories
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12 • Symbols
Chapter 12
Symbols
Individual details of the symbols in this chapter may deviate from your product. Not all
symbols may necessarily appear on your device or its packaging.
Symbol Explanation
Caution, consult accompanying documents
Catalogue number
Serial number
Manufacturer
Date of manufacture
Keep away from sunlight
Keep dry
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Temperature limit
Humidity limitation
Atmospheric pressure limitation
Quantity (x)
X
Follow instructions for use
Foot switch
ECB Erbe Communication Bus

Used to exchange data between Erbe units.
Equipotentiality
Refers to the grounding terminal.
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12 • Symbols
Symbol Explanation
Off, On
Defibrillation-proof type CF applied part

The applied parts of the unit (e.g. instrument sockets) are pro-
tected against the effects of defibrillator discharge.
HF isolated patient circuit

The danger of leakage currents and therefore the danger of burns
is substantially reduced for the patient.
Non-ionizing electromagnetic radiation

A unit that bears this symbol does not transmit ionizing electro-
magnetic radiation. Interference may occur in the vicinity of the
unit.
The product must be disposed of separately.
European conformity marking

CE
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User Manual ERBEJET - 2

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USER MANUAL

HYDROSURGERY 80110-801 2019-01

MEDICAL - GENERAL MEDICAL EQUIPMENT

2 Description of the Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

3 Working with ERBEJET 2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

Connecting suction module ESM 2, connecting the applicator to the pump

4 Status Messages, Error Messages . . . . . . . . . . . . . . . . . . . . . . . . . . 37

Electrical installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43

6 Disassembly, Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . 45

8 Information on electromagnetic compatibility (EMC) . . . . . . . . . . . 51

9 Maintenance, Customer Service, Warranty, Disposal . . . . . . . . . . . . 55

10 Combination with other equipment, Third-party accessories . . . . . 57

result in minor or moderate injury.

Meaning of the note

Who must read this User Manual?

Compliance with safety information

Structure of safety instructions

Operating errors and incorrect installation by persons without training

 In the event of uncertainties or if you have any questions, please

Risks due to the environment

Unsuitable temperature or humidity in transit or storage

The patient can be infected by the use of a non-sterile separating

Defective unit, defective accessories

Interference caused by the unit

The unit may fail or not perform properly.

Safety information for use of ERBEJET 2

against the effects of a defibrillator discharge.

Controls on the front panel

Power (2) Power switch

Pump shaft (4)

Selection buttons (L1) (L2) (L3) (R1) (R2) (R3)

Controls on the back

Sockets (1) Footswitch socket

Potential equalization (4) Potential equalization terminal

Power connection (6) Power connection

Connecting suction module ESM 2, connecting the applicator to the

validate liability on the part of Erbe Elektromedizin GmbH.

Attaching the mounting bracket

 Equip the bracket with a mounting bracket.

 Hang the suction container on the mounting bracket.

Inserting the suction bag

 Insert the suction bag into the suction container.

1. Connect the vacuum hose with the membrane filter.

Connecting the applicator to the

 Use aseptic techniques when you connect the applicator connec-

Selecting program, Inserting pump unit, Connecting separating

2. You will then see a selection list of programs.

Inserting the pump unit into

Connecting the separating medium

Priming the pump unit and

Mounting suction hose of applicator to suction container

1. Attach the adapter to the connection for the suction hose.

2. Attach the suction hose to the adapter.

Window settings, Selecting effect, Setting suction

The following parameters are stored in each program:

 Use personal protective equipment, e.g. a face mask and splash

Activating with the single-pedal

only water jet Off yes

continuous suction independent Cont. no

water jet + suction independent Cont. yes

water jet + suction Setting pedal + run-on yes

water jet + suction + run-on Setting pedal + run-on yes

Activating with the dual-pedal