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Applicable for use outside the US

PRIOR TO CHANGE
Technical Specifications
Konelab 30
Konelab 30 is a random access clinical
chemistry system for routine and
special chemistries, including specific
proteins, electrolytes, therapeutic
drugs, and drugs of abuse tests.
The broad range of CE marked applica-
tions can be complemented with user-
definable tests.

Throughput Reagents
Workload dependent, being in typi- Continuous access to reagents
cal routine use up to 300 tests/hour. without interrupting test processing.
Time to first result is typically 3 to 12 Automated indentification by integrat-
minutes. ed barcode reader. Real time reagent
status clearly displayed. Up to four
Samples
reagent additions / test possible.
Continuous access to samples with-
ON-BOARD STORAGE:
out interrupting test processing. 45 positions in the refrigerated
Optional automation interface, KUSTI. reagent compartment.
ON-BOARD CAPACITY: REAGENT VIALS: 10, 20 and 60 ml
84 routine samples and 6 STAT sam- REAGENT VOLUMES: 2-250 µl; typi-
ples - 6 segments with 14 positions cally 120 - 200 µl.
per segment. Integrated barcode
reader and cup/tube recognition. Cuvettes
SAMPLE CUPS AND TUBES: Discrete disposable 12-cell cuvette.
0.5 ml and 2.0 ml cups, 5 ml and
Continuous access to cuvettes with-
7 ml tubes, 10 ml tubes with tailored
out interrupting test processing.
segments.
ON-BOARD CAPACITY:
SAMPLE TYPES: Serum, plasma,
600 measurement cells - 50 multicell
urine, CSF.
cuvettes with 12 reaction cells, typi-
SAMPLE VOLUMES: Possible range
cally up to 2 hours walk-away time.
1-120 µl ; typically 2-15 µl and 50 µl for
Na+, K+ and Cl- ISE tests.
Technical Specifications
Konelab 30
Applicable for use outside the US

Calibration Photometric Measurement Data Management


Linear, non-linear or bias calibra- Single channel interference filter Windows® XP workstation with
tion. Method-dependent use of photometer with beam splitting graphical user interface.
individual calibrators or automati- reference - 11 fixed filters, others Data input online, by mouse or key-
cally diluted series from a stock available upon request. board. Different language versions
calibrator. Automatic repeat for bias SPECTRAL RANGE: 340-800 nm. available.
correction available. MEASUREMENT TEMPERATURE: SAMPLE BARCODES IN USE:
ON-BOARD CAPACITY: 37 oC Code 128, Code 39, USS Codabar,
20 positions in the cooled area of MEASUREMENT PRINCIPLES: Interleaved 2 of 5.
the sample disk, also possible to Colorimetric, turbidimetric LIS INTERFACE: ASTM 1394-91 or
load them into segments. MEASUREMENT MODES: KONE Online.
Kinetic, end-point HARDWARE INTERFACE: RS-232
Quality Control KINETIC MEASUREMENT: RESULT REPORTS: Collated by
Real time QC with multiple, 30 sec to 60 min, max 12 points patients, manual entry of off-line
user-definable Westgard rules. LIGHT SOURCE: Halogen lamp results allowing for fully collated
Programmable control interval. with linear absorbance range of result reports, results calculated
QC chart printouts, daily and cumu- 0-2.5 A, resolution of 0.001 A and from both measured and off-line
lative reports. reproducibility of SD≤0.005 A results. Automatic or ‘on request’
ON-BOARD CAPACITY: at 2 A. printouts, automatic STAT report-
19 positions in the cooled area of ing. Abnormal values and repeats
the sample disk, also possible to ISE Measurement in the flagged automatically.
load them into segments. model Konelab 30i DATA STORAGE: Long term stor-
Direct potentiometry. Electrodes age of patients with demographics
Sample and Reagent for Na+, K+ and Cl-; upon request
Dispensing including test and QC results and
Li+,Ca2+ and pH. calibrations.
Externally and internally rinsed USABLE RANGE: (mmol/l)
single probe dispensers equipped serum, plasma: Dimensions and Weight
with level sensing. K+ 2.0 - 10 Width 120 cm, depth 79 cm, height
Dispensing with precision syringes Na+ 100 - 200 115 cm, weight 200 kg. Separate
driven by stepping motors. Cl- 55 - 150 workstation table.
REACTION END VOLUME: Ca2+ 0.5 - 6.0
100-250 µl. pH 6 - 8.5 Power Requirements
SAMPLE CARRY OVER: <1%. serum: 0.7 kVA, 100-230 V ±10%,
REPRODUCIBILITY: Li+ 0.2 - 4.0 50-60 Hz ±5%. Power failure secu-
CV less than 2% for sample urine: rity (battery back-up facility).
volumes ≥2 µl and for reagent K+ 20 - 200
volumes >5 µl. Distilled Water Consumption
Na+ 20 - 200 Typically <1.5 l/h
Dilutions On-board storage with no external
Automatic sample predilution. connections required.
Environmental Conditions
Automatic postdilution with both
Operating temperature range of Ordering Codes
high and low secondary dilution
ratios. Ability to add the value of 15-32 °C; humidity 40-85% (non 981851 Konelab 30i
manual pre-dilution for the result condensing). 981861 Konelab 30i with KUSTI
calculation. 981850 Konelab 30
DILUTION RATIOS: up to 1+120 981860 Konelab 30 with KUSTI
Regulatory NOTE: The information and techni-
CODE 895290_Q CONFORMITY WITH: cal specifications are subject to
04 / 2007 98/79/EC IVDMD Directive. change without notice.

Clinical Diagnostics Finland Tel.: +358 9 329 100


Ratastie 2, P.O. Box 100 Fax: +358 9 3291 0300
FI-01621 Vantaa www.thermo.com/konelab

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