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Americon Notionol Stondord-

Minimum Requirements for


Workploce First Aid Kits ond
S, pplies
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ANSI/ISEA 2308.1-2009
Revision of
ANS| 2308.1-2A03
American National Stapdard-
Minimum Requirements for
Workplace First Aid Kits and Supplies
Secretariat
International Safety Equipment Association
Approved May 8, 2009
American National Standards Institute, Inc.
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Ameriqan
Nationhl
Standard
An American National Standard implies a consensus of those substantially
concerned with its scope and provisions. An American National Standard
is intended as a guide to aid the manufacturer, the consumer, and general
public. The existence of an American National Standard does not in any
respect preclude anyone, whether he has approved the standard or not,
from manufacturing, marketing, purchasing, or using products, processes,
or procedures not conforming to the standard. American National
Standards are subject to periodic review and users are cautioned to obtain
the latest edition.
CAUTION NOTICE: This American National Standard may be revised or
withdrawn at any time. The procedures of the American National
Standards Institute require that action be taken to reaffirm, revise, or
withdraw this standard no later than five years from the date of publication.
Purchasers of American National Standards may receive current
information on all standards by calling or writing the American National
Standards lnstitute.
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International Safety Equipment Association
1901 North
lVloore
Street, Suite 808, Arlington, Virginia 22209
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Copyright 2009 by International Safety Equipment Association
All rights reserved.
No part of this publication may be reproduced
in any form,
in
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Foreword
(This Foreword is not part of American National Standard ANSI/ISEA 2308.1-2009).
leading industry stakeholders, has developed this standard, updating and expanding ANSI/lSEAZ3O8.1-
2003, to provide guidance for minimum performance levels of first aid kits for all types of uses qnd
situations in the work environment. Member companies of the ISEA Industrial First Aid Group ihclude:
ARl, 3M Company, MSA and North by Honeywell.
Kits in compliance with this standard will provide a basic range of products to deal with most types of
injuries encountered in the workplace. The assortment of required contents was developed bafed on
treatment for the following potential injuries: major wounds, minor wounds (cuts and abrasions), minor
burns and eye injuries. Significant updates incorporated into this version include the designation of new
kit types and expansion of the required supply list to include a first aid guide. The recommendQd supplies
list has been expanded to include hand sanitizers in response to updated hygiene protocols anp provide
additional volume of eye/face wash. The kit label has been redesigned to draw specific attenti{n to fact
that each workplace is unique and, as such, may necessitate the availability of additional first
{id
supplies.
Suggestions for improvement of this standard are welcome. They should be sent to ISEA, 19q1 N. Moore
Street, Suite 808, Arlington, VA 22209, isea@safetyequioment.org.
This standard was processed and approved using consensus procedures prescribed by the
National Standards Institute. The following organizations were contacted prior to the approval
standard. Inclusion in this list does not necessarily imply that the organization concurred with
submiftal of the proposed standard to ANSI.
this
American Association of Occupational Health Nurses
American Contractors Insurance Group
Atlas I ndustrial Contractors
Baker Hughes
Mr. Greg Easter
Federal Aviation Administration
Georgetown University
International Safety Equipment Association
National Safety Council
North Carolina Deot. of Health and Human
Pick International, Inc.
Prepa Electric Company
Safety Equipment Institute
State of California
-
Occuoational
Div.
Think Safe, Inc.
and Health
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Contents
1.
2
3.
4.
PAGE
6.
j
Recommended First Aid Kit Supplies .............3
6.1 Required Supplies ..............3
6.1.1 Minimum Performance Criteria for Required Supplies .........3
6.2 Recommended Supplies. ..5
6.2.1 Minimum Performance Criteria for Recommended Supplies ...................5
Unit First Aid Kits ........................7
7.1 General ...........7
7.2 Packaging for Individual Basic Units ........... ...............7
7.3 Unit Packaging Labeling .........................7
First Aid Kit Marking and Labeling ..................7
AppQndix A: First Aid Guide.... ........... 9
8.
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Workplace First Aid Kits and Supp
American National Standard
Minimum Requirements for
1. Scope and Purpose
This standard establishes minimum
performance
requirements for first aid kits and their supplies
that are intended for use in various work
environments. Because each work environment
is unique, it is expected that the required
products will be supplemented with additional
supplies and quantities based upon the
consultation and recommendation of a person
competent in first aid and cognizant of the
hazards found in the particular work
environment and upon the number of persons
who may need first aid at one time. Persons
determining the content of first aid kits should
additionally consult federal, state and local
requirements regarding the types and quantities
of material to be included.
2. Compliance
To be in compliance with this standard, first aid
kits must contain the required supplies of
Section 6.1 and meet all other applicable
requirements in their entirety. This standard
anticipates that additional first aid supplies will
be included to augment the kit, based upon the
specific hazards existing in a particular work
environment. The inclusion of workplace-
specific first aid supplies does not, in and of
itself, place a first aid kit outside the purview of
this standard. A first aid kit containing a
recommended supply that is specifically
addressed by this standard must comply with
the minimum performance criteria established
for such supplies under Section 6.2.
The choice of first aid supplies should be made
by a person competent in first aid and cognizant
of the hazards found in the particular work
environment.
All labeling and marking reguirements of this
standard represent the manufacturer's
declaration of compliance with this standard.
The accuracy of the claim is therefore solely the
responsibility of the party marking the product.
All labeling and markings shall be legible and
permanent. Where adhesive labels are used
they shall not be easily removed.
Bandage. A strip of material used tolcover a
wound or hold a compress in place.
Breathing Barrier. A personal safe
that prevents any contact between th
ANSr/tSEA 2308j-2009
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3. Definitions
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Analgesic. Medications approved b{ the FDA
as pain reliever/fever reducer for ove{-the-
counter use. I
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Antiseptic. A substance that inhibit! the growth
of microorganisms on human skin.
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adminstrator and the victim. Also kn wnasa
CPR barrier.
Compress. A sterile absorbent pad.
device
CPR
around
used to
First Aid. lmmediate treatment administered to
an injured person when professionalpedical
care is not readily available.
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First Aid Kit. A container including a quantity of
first aid supplies,
Roller Bandage. A bandage made gauze or
gauze-like materials; generally
a body part over a dressing.
Swab. A single-use crushable,
sealed ampoule with an applicator
clean and/or apply a solution.
Towelette. A single-use, sealed,
material used to clean and/or apply solution.
Unit First Aid. A system of first aid
materials in uniform sized packages
one or more applications of first aid
Wipe. A small towelette.
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ANSr/rSEA 2308.1-2009
4.1 Genieral
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All first aid kits meeting the requirements of this
standard shall incorporate a means to contain
and protect kit supplies while permitting easy
accessibility.] First aid kits shall be classified as
Table 1. Classification and Characteristics of First Aid Kits
Type I, TypQ ll Type lll or Type lV as described
in Sections
{.2
thorugh 4.5 and summarized in
Table 1.
4.2 Typf I
Type | first aid kits are intended for use in
stationary, iqdoor settings where the potential for
damage of klt supplies due to environmental
factors and rpugh handling is minimal. Type I
first aid kits shall have a means for mounting in
a fixed and are generally not intended to
be oortable.
NOTE: T applications for Type | first aid kits
may include, are not limited to, the following:
general use, an office setting or a
facility. First aid cabinets would
generally fall the Type I classification.
4.3
Type llfirst kits are intended for use in
portable, i settings where the potential for
damage of
factors and
supplies due to environmental
handling is minimal.
NOTE; applications for Type ll first aid kits
may include, are not limited to, the following:
general use, an office setting or a
facility.
ill 4.4
Type lll first
{iO
kits are intended for portable
use in mobile, indoor andlor outdoor settings
pote damage suppl
due to environmentalfactors is not probable.
Type lll kits shall have a means to be mounted
in a fixed
position
and shall have a water
resistant seal.
Note: Typical applications for Type lll first aid kits
may include general indoor use and sheltered outdoor
use.
4.5 Type lV
Type lV first aid kits are intended for portable
use in the mobile industries and/or outdoor
seftings where the potential for damage to kit
supplies due to environmental factors and rough
handling is significant. Type lV kits shall have a
means to be mounted in a fixed position.
NOTE: Typical applications for Type lV first aid kits
may include, but are not limited to, the following: the
transportation industry, the utility industry, the
construction industry, and the armed forces.
5. Performance Requirements for
Type lV Kits
5.1 Corrosion and Moisture Resistance
After being subjected to the corrosion test as
specified in Section 5.1.1, the kits shall not be
difficult to open or show evidence of moisture on
the inside.
Corrosion and Moisture Resistance
Three kits shall be tested for corrosion and
moisture resistance in accordance with ASTM
8117 Standard Practice for Operating Sa/f Spray
(fog) Apparafus for a duration of 480 hours (20
days). The exterior surface of each sample shall
5.1.1
Test
Page2
Lice,'rsdd tc Jeffre!
Type Use Portable Mountable
Water
Resistant
Waterproof Performance
Kit
Examoles
lnr oor X Cabinets
tl In{oor X Soft Packs
llt
Indoor/
Outdoor
X X X Plastic Kits
IV
Indoor/
Outdoor
X X X Section 5 Metal Kits
4. c of First Aid Kits where the
potential
for damaqe of kit supplies
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be carefully blotted dry and the container shall
be opened. Each sample shall be evaluated for
ease of operation. The interior of the kit
container shall be examined for evidence of
moisture. Difficult operation or any evidence of
moisture is sufficient cause for failure.
5.2 lmpact Resistance
After being conditioned and subjected to the
drop test as specified in Section 5.2.'1
,
the kits
shall not open or be rendered difficult to open. lf
any of the three test samples cannot be opened
easily after impact or opens as a result of
impact, the kit fails the test.
5.2.1 Drop Test
The purpose of the drop test is to ensure that
the first aid supplies remain in the container.
Test sample shall consist of a first aid container
loaded with the appropriate weight as noted
below:
.
1 lb for'10 unit container
.
1.5lb for 16 unit container
.
2 lb for 24 unit container
.
2.5 lb for 36 unit container.
Three samples shall be conditioned hot at 120'F
(49'C) for a minimum of 2 hours, and three
samples shall be conditioned cold at 0'F (-18'C)
for a minimum of 2 hours.
Each conditioned sample shall be subjected to
the following drop test within 1.0 minute of
removal from the conditioning environment.
Each sample shall be dropped freely from a
vertical height of 48 in. (120 cm), as measured
from the bottom of the kit sample, onto a hard
flat rigid surface such as concrete or a surface of
equivalent hardness. Each sample shall be
dropped once, each on a different corner of the
case. For first aid kits that do not have corners,
each sample shall be dropped on a different
location. The kits shall be examined after impact
to determine if the kit is opened or is capable of
being opened.
ANSI/ISEA
First Aid Kits Supplies
First aid kits should be regularly i
ensure completeness, condition of and
expiration dates to maintain with this
6.
date should be removed from the kit and
replaced. Additional quantities should to be
added as needed to address the hazdrds of a
particular work environment.
6,1 Required Supplies
All Type 1, Type ll, Type lll and Type
fV
first aid
kits conforming to the requirements o! this
standard shall contain the first aid suflplies
indicated in Table 2. The quantity, dirhensions,
or volume listed for each supply is the minimum
for compliance with this standard. Larger-sized
supplies that meet or exceed the perfprmance
requirements of Section 6.1.1 are cortsidered
equivalent.
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standard. Supplies shall be natural
free. Any supply beyond its marked
sealed, and sterile.
NOTE: This is a major wound
6.1.1 Minimum Performance Critgria for
Required Supplies
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6.1.1.1 Absorbent Compress. Each
absorbent compress shall be at least 32 sq. in.
(206 sq. cm)with no side smaller than 4 in. (10.1
cm) with at least an equivalent absor$ency of
2.37 fl. oz. (70 g) of water as defined
by
tn"
gauze section in ASTM D1117 Standprd Guide
for Evaluating Nonwoven Fabrlcs. Edch
compress shall be individually packaged,
latex
ration
to be used
to apply pressure and stop bleeding. A
folded to a minimum 4 x 8 in. fij.1 x20. cm) size is
acceptable if it meets the absorbency
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ANSyrsEAl*,-r*,
Table 2. Required Supplies
Supply and Minimum Size or Volume
Performance
Requirement
Section
Minimum
Quantity
Absorbent Compress, 32 sq. in. (206 sq. cm), with no side smaller than 4
in. (10 cm)
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6.1.1.1
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Adhesive Bandages, 1 x 3 in. (2.5 x 7.5 cm) 6.1.1.2 16
Adhesive Tape, 3/8 in. x 2.5 yd. (2.3 m) total 6.1.1.3 1
Antibiotic Tr atment, 0.14 fl oz (0.5 g) application 6.1.1.4 o
Antiseptic,
(
14 tl. oz. (0.5 g) application 6.1.1.5 10
Burn Treatment, 1132 oz. (0.9 g) application 6.1.1.6 b
First Aid Guide 6.1.1.7
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Medical Exam Gloves 6.1.1.8 2 pair
Sterile pad, x 3 in. (7.5 x 7.5 cm) 6.'t.1.9 4
Triangular E rndage, 40x40 x 56 in. (101 x 101 x142cm) 6.1 .1 .1 0
6.1.1.2 Ad Each adhesive 6.1.1.4 Antibiotic Treatment. Each antibiotic Bandage
bandage shall consist of a non-adherent
absorbent pad attached to the central area of a
strip of material. The adhesive strip
shall be 3.0 ! 1116 in. (76 mm t 1.6 mm)by
1.0 in. t 1l3Jin. (25.4 mm t 0.8 cm). The
absorbent odd shall have an area between 0.65
and 1.0 sq. ifi. (420 - 645 sq. mm). The ratio of
the greater
ffid
dimension to the lesser pad
dimension be between
'1.0
and 2.0. The
adhesive
treatment shall meet the applicable
requirements for antibiotic treatment as defined
in the current edition of the USP/NF. Each
treatment shall be packaged in individual use
appf ications containing at least .14 fl oz. (0.5 g)
of ointment. Each individual-use application
shall not be reusable.
6.1.1.5 Antiseptic. Each antiseptic shall meet
the requirements of all applicable FDA
requirements shall be contained in an individual-
use application containing at least 0.14 fl. oz.
(0.5
S)
of antiseptic. Each individual-use
application shall not be reusable.
NOTE: Commonly used applicators are swabs, wipes
and towelettes. Spray containers with a minimum of
ten 0.14 fl. oz. (0.5 g) applications are acceptable to
meet this requirement.
6.1.1.6 Burn Treatment. Each burn treatment
shall be a water soluble compound packaged in
individual-use applications containing at least
1132 oz. (0.9 g).
NOTE: Spray containers with a minimum of six 1132
oz. (0.9 g) applications are acceptable to meet this
requirement. Burn treatment, as required here, is
intended to address the treatment of minor burns.
erial shall have a moisture vaoor
rate of at least 500 gm/mz per 24
hours over its entire area in accordance with
ASTM E96
lfandard
Test Methods forWater
Vapor Transmiss,bn of Materials. Protective
material shall cover the adhesive material and
pad in such a manner as to prevent
contamination of the pad. The protective facing
material shall not impair the adhesiveness of the
adhesive maferial and shall be easily removed.
Each bandage shall be individually packaged,
sealed and sterile.
6.1.1.3 Adhesive Tape. Adhesive tape shall
be at least 3/F in. (9.5 mm) wide and a minimum
of 2.5 yd (Z.3jm) long and meet the applicable
requirementslfor adhesive tape as defined in the
current edition of the USP/NF.
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NOTE: Multiplp rolls may be used to meet the
minimum requirement ot 2.5 yd (2.3 m) of tape.
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Table 3. Dimensions of Bandage Compress (t
ANSIiISEA
1/8 in.
;
t 0.32 cm)
6.1.1.7 First Aid Guide. Guidance for
immediate care given to a victim of injury or
sudden illness until more advance care, if
needed, shall be included in the kits. At a
minimum, the guide shall include the areas
outlined in Appendix A.
6.1.1.8 Medical Exam Gloves. Gloves shall
meet the requirements of FDA regulation 21
CFR 800.20 for medical grade gloves.
6.1.1.9 Sterile
pad. Each sterile pad shall be at
least 3 x 3 in. (7.5 x 7.5 cm) in size and absorb
at least 0.56 fl. oz. (2 g) of water as determined
by ASTM D1117 Standard Guide for Evaluating
Nonwoven Fabrics. Each sterile pad shall be
individually packaged, sealed and sterile.
6.1.1.10 Triangular Bandage. Each bandage
shall be made from muslin at least 60/48 weave
or a material of equivalent mechanical strength.
When unfolded, the outer dimensions of the
bandage shall be at least 40x40 x 56 in. (101 x
101 x 142 cm}
6.2 RecommendedSupplies
In addition to the required supplies listed in
Section 6. 1 .1
,
optional supplies and sizes should
be included, to augment a kit based upon the
specific hazards existing in a particular work
environment. Supplies specifically addressed by
this standard shall meet all of the applicable
criteria in Section 6.2.1. ltems not addressed by
this standard shall be in compliance with
standards or regulations, where applicable,
established by the U.S. Food and Drug
Administration (FDA), the current edition of the
U.S. Pharmacopoeia/National Formulary
(USP/NF) or any other equivalent strandard
writing body.
single dose, tamper evident,
labeling as required by FDA
with full
should contain no ingredients which
cause drowsiness.
6.2.1.2 Bandage Compress. Each bandage
compress shall consist of an absorbent, non-
adherent pad substantially free from lbose ends
and raveling and constructed from a material
having at least the equivalent absorbfncy of
'16
thicknesses of Type lll (28124) absorbent gauze
as defined by the current edition of the USP/NF.
The compress shall be securely attached to a
continuous bandage substantially freg from loose
ends and raveling, constructed from /naterial
having the equivalent strength of Type | (44136)
gauze. The bandage shall be pl
provide easy opening and appli
bandage compress shall be
packaged, sealed and sterile.
6.2.1 MinimumPerformance
Recommended Supplies
6.2.1.1 Analgesic (Oral). Oral
included in a first aid kit shall be
comoresses shall conform to one of
shown in Table 3.
6.2.1.3 Breathing Barrier. The
shall be a single use disposable
Ina
and
known to
or rolled to
Each
SIZES
barrier
device
current valid 510 (k). The device shall provide
protection from direct contact with bodily fluids by
way valve, filter medium or other
method. Each barrier shall be
easily opened container, clearly
name of the device, together with
instructions for use.
the need for other items, consideration should be given
to state or local governing authority related to breathing
7.5 x7.5 7.5x152 7.5 x 15
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barriers and training on these devices.
ANS / sEAZL'B
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6,2.1.4 Burn Dressing. Burn dressings shall
be a gel-soal6ed pad made of a material that
avoids fiberslfrom becoming imbedded in the
burn wound. lGel material shall be water
soluable. Each dressing size shall be at least 12
sq. in. (77.4 sq. cm)and shall be single use.
6.2.1.5 Cold Pack. Each cold pack shall be at
least 4 x 5 in](10 x 12.5 cm) in size and shall
reach a tempbrature between 20 - 40'F (-6 -
4'C) within 10 seconds of activation. The cold
pack shall maintain a temperature between 20 -
40'F (-6 - 4'Q) for a period of at least 10
minutes. Colb packs shall activate under normal
hand pressure and shall not leak under normal
conditions of pse.
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6.2.1.6 Eye
$overing.
Eye covering(s) shall
have the ability to cover both eyes, an area of at
least 2.9 sq. in. (19 sq. cm) per eye, and
have at least the absorbency of absorbent gauze
as defined by the current edition of the USP/NF.
The eye covering shall be free of loose threads
and raveled edges. Each eye covering shall be
individually packaged, sealed, and sterile.
NOTE: The minimum requirement for eye covering
shall be two eye pads or a single covering for both
eyes.
6.2.1.7 Eye/Skin Wash. A minimum of 4 fl. oz.
(118 ml) of a sterile, isotonic, buffered solution as
specified by the FDA in 21 CFR 349 shall be
contained in at least 0.5 fl. oz. (15 ml) individual-
use applicalions.
NOTE: Where the work environment dictates the
possible need for copious amounts of fluid, users
should refer to ANSI/ISEA 2358.1 American National
Standard for Emergency Eyewash and Shower
Equipment.
conform to eqch eye cavity. The covering shall
have a thicknpss of at least 1/4 in. (0.64 cm)
when not conlpressed. Each eye covering shall
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Table 4. Minimum Quantity Requirements for Unit Padkaging
Unit first aid supply
Minimum Size
or Volume - US
Minimum Size
or Volume {metric)
Supply quantity
ner lrnil nankada
Absorbent Compress
32 sq. in. 206 sq. cm 1
Adhesive Bandage 1x3in. 2.5x7.5cm 16
Adhesive Tape 2.5 yd (total) 2.3 m
'l
or2
\ntibiotic Treatmenl 0.14 fl oz, 0.5 g o
Antiseptic Swab 0.14ll oz. 0.5 g 10
Antiseptic Wipe 1x1in. 2.5x2.5 cm 10
\ntiseotic Towelette 24 sq. in. 157 sq. cm 10
Bafidage Compress (2 in.) 2x36in. 5x91 cm 4
Bandage Compress (3 in.) 3x60in 7.5 x 152 cm 2
Bandage Compress (4 in.) 4 x72 in. 10 x 183 cm 1
Breathing Barrier 1
Burn Dressing 4 x4 in. 10 x 10 cm 1
Burn Treatment 1132 oz o9g o
Cold Pack 4x5in. 10 x 12.5 cm 1
Eye Covering, with means
of attachment
2.9 sq. in. 19 sq. cm z
EyelSkin Wash 4 fl. oz. total 118 ml total 1
EyelSkin Wash & Covering,
witlh means of attachment
4 fl. oz. total
2.9 so. in.
118 ml total
19 so. cm z
Gloves 2 pail
Hand Sanitizer 1132 oz.
llOa
v.v
v
6
rller Bandage (4 in.) 4in.x4yd 10 x 366 cm 1
lller Bandage (2 in.) 2in. x 4yd. 5x366cm z
Sterile pad 3x3in. 7.5x7.5cm 4
Triangular Bandage 40x40x56in. 101x 101 x142cm
6.2.1.8 Hand Sanitizer. Hand Sanitizers shall
be water soluable with a minimum 61% ethyl
alcohol as the active ingredient.
NOTE Spray containers with a minimum of six 1/32
oz. (0.9 g) applications are acceptable to meet this
reouirement.
6.2.1.9 Roller Bandage. Each roller bandage
shaf f be at least 2 in. (5 cm) wide and at least 4
yd (365 cm) long (non-stretched). Each
bandage shall be constructed from a material at
least the equivalent strength of Type I USP 28-
NF23 (44136) gauze as defined by the current
edition of USP/NF. Each bandage shall be
individually packaged and sealed.
NOTE: A conforming bandage that can stretch to at
least 4 yards (365 cm) may be used in place of roller
bandage.
7. Unit First Aid Kit
7.1 General
Unit first aid kits shall be designated as by Type
in accordance with Section 4. Unit first aid kits
shall meet the all the applicable requirements of
Section 6.
7.2 Packaging for Individual Basic Units
Where a minimum individualfirst aid supply is
packaged for a unit first aid kit, it shall meet the
specifications in Table 4 and the applicable
performance criteria in Sections 6.1.1 and 6.2.1.
7.3 Unit Packaging Labeling
All unit packages shall be labeled with at least
the following information:
(1) The name of the item shall appear at
least on the top panel and one end
panel,
(2) The quantity contained,
(3) Instructions and/or illustrations for
proper use of supplies,
(4) Name of manufacturer, packager,
and/or distributor, and place of
business,
(5) All unit packages shall be labeled in
accordance with the requirements of the
Food, Drug & Cosmetic Act, and all
other applicable state and federal
regulations.
ANSI/ISEA
Unit packages shall include the
coding:
r Blue - Antiseptics
. Yellow - Bandages
o Red - Burn Treatment
o
Orange - Personal Protective E
.
Green
-
Miscellaneous
NOTE: Size and manner of color
discretionary but should be i
I
8. First Aid Kit Marking and Labeling
Each kit and/or location shall be vislUt[ marked
as a place where first aid supplies are locatec.
Each complete first aid kit shall
information shown in Figure 1,
point font.
the
in at least 6
Page 7
prohibrted.
Lrcgrrsed to Jeffrey Writef. A\Sl l:cf*r order * X_219423. nr*rnloaded 4!1!2011 1:1,t PLl. Single user license only. Coi:ying and
ANSYISEA 1-2009
Figure 1. ANSI/ISE A 2308.1 -2009 Label
ANSI/ISEA 2308.1-2009 Type l, ll, lll or lV
Caution! This kit meets ANSI/lSEAZ.308.1-2009 only when required minimum fill
is maintained with first aid
products
marked "ANSUISEA
2308.1-2009."
Required
1 First Aid
1 Absorbent 4x8in.min.
1x3in. 16 Adhesive
1 Adhesive 2.5yd.
10 Antiseptic
[reatment
Applications 0.5 gm. each
6 Burn Trea Applications 0.9 gm. each
4 Sterile Pads 3 x 3 in. min.
2 Pair Medical Exam Gloves
1 Triangular Bandage 40 x 40 x 56 in. min.
6 Antibiotic Treatment Applications 0.5 gm. each
Recommended Supplles
Analgesic (Oral)
Bandage Compress 2 x 36 in. min.
Breathing Barrier, single use
Burn Dressing 12 sq. in. min.
ColdPack4x5in.min.
Eye Covering 1/4 in. thick min.
Eye/Face Wash, sterile 4 fl. oz. min
Roller Bandage 2 in. x 4 yd. min.
Hand Sanitizer, 0.9 gm. min
The describe( kit may be suitable for some businesses. However, the adequacy of the contents for hazards of each
work environrhent should always be evaluated by competent personnel. For a variety of operations, employers may
find that additional first aid supplies and kits are needed.
Page 8
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ANSI/tSEA 2308.1-2009
Appendix A: First Aid Guide
The inclusion of a first aid guide in a first aid kit is required per Section 6.1 of this standard. Al
minimum, the information below shall be included in the guide. The manner in which such infc
conveyed is left to the discretion of the manufacturer.
is
First Aid Guide Areas
Emerqencv steps of assessinq the scene and
person,
callinq 9-1-1 or location emerqencv number
Establishinq responsiveness
Establishinq and maintaininq an open and clear airwav
Performinq rescue breathinq
Treatinq airwav obstruction in a conscious victim
Performino CPR
Usinq an AED
Recoonizino the sions and svmotoms of shock and orovidino first aid for shock from illness or niurv
Assessing and treating a victim who has an unexplained change in level of consciousness or sudden
illness
Controllinq bleedinq with direct
pressure
Poisonino
Responding to medical emergencies
Chest pain
Stroke
Breathing problems
Anaphylactic reaction
Hypoglycemia in diabetics taking
Seizures
Reduced level of consciousness
lmoaled obiect
insulin
Wounds
Assessment of and first aid wounds including abrasions, cuts, lacerations, punctures,
amputations and crash injuries
Principles of wound care including infections precautions
Princioles of bodv substance isolation. universal
precautions
and use of PPE
vulsions,
Burns
Assessment of the severity of a burn
Recoqnizinq whether a burn is thermal, electrical or chemical and the appropriate first rid
Temperature extremes
Exposure to cold, including frostbite and hypothermia
Exposure to heat, includinq heat cramps, heat exhaustion and heat stroke
Musculoskeletal injuries
Fractures
Sprains, strains, contusions and cramps
Head, neck, back and spinal iniuries
Eve iniuries
Mouth and teeth injuries
Oral iniuries, lip and tonque iniuries, broken and missing teeth
Bites and stings
Human and animal bites
Bites and stinos from insects: instruction in first aid treatment for anaphvlacsis
Lr.ensed io ieffrey Vv.-riiei ANSji slore of{ier # X_2-19.125. Downioae;d 411!21i1
' 't::.:i Pil. S;lrgie .lser license oniy. Copying and
Page 9
prohib(6d.
ANSr/ISEA 2808.1-2009
Reference
Page 10
Licensed to Jeffrev
American Red Cross-First Aid-Responding to Emergencies Revised 4th edition 2006,
lsBN 1-58480-322-3
ANSI/ISEA
f358.1
,
American National Standard for Emergency Eyewash and Shower Equipment
ASTM BllTlStandard Practice for Operating Salt Spray (fog) Apparatus, 2007
ASTM D111V Standard Guide for Evaluating Nonwoven Fabrics,2001
ASTM E96 $fandard Test Methods forWater VaporTnnsmission of Mafen'als, 2005
Title 21, Co{e of Federal Regulations (CFR) Part 800.20, Patient examination gloves and surgeons'
gloves; sample plans and test method for leakage defects; adulteration
United States Pharmacopeia
-
National Formulary
ANSI store orcier # X_219423. Downloaded 4 1 2011 1:'14 PM. Single usef iicense only. Copying and networking prohibited

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