ABL80 SC80

SC80 200/60 for FLEX, CO-OX,OSM version

Registry build 21.09.26
1manufacturer
66catalogue numbers in this listing
13510(k) clearances naming this product code
14recalls on this code

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code CHL
Manufacturer City Province Registered as Device types
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Record

Regulatory record for ABL80 SC80
Listed by Radiometer Medical APS, Denmark
FDA product code CHL
Device type Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Device class Class 2
Regulation 21 CFR 862.1120
Establishment Complaint-file establishment, Manufacturer
Record published 2016-09-01
Record revised 2026-04-09 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 5 to 25 °C
Distribution end date 2026-04-08

Catalogue Numbers

Catalogue numbers for ABL80 SC80
Catalogue number Size Status
945-719 In distribution
945-725 In distribution
945-674 In distribution
945-806 In distribution
945-670 In distribution
945-714 In distribution
945-710 In distribution
945-681 In distribution
945-843 In distribution
945-722 In distribution
945-668 In distribution
945-728 In distribution
945-685 In distribution
945-727 In distribution
945-706 In distribution
945-707 In distribution
945-676 In distribution
945-715 In distribution
945-672 In distribution
945-726 In distribution
945-702 In distribution
945-770 In distribution
945-671 In distribution
945-712 In distribution
945-666 In distribution
945-713 In distribution
945-708 In distribution
945-701 In distribution
945-677 In distribution
945-665 In distribution
945-690 In distribution
945-680 In distribution
945-700 In distribution
945-675 In distribution
945-673 In distribution
945-731 In distribution
945-704 In distribution
945-678 Withdrawn
945-721 Withdrawn
945-720 Withdrawn
945-667 Withdrawn
945-711 Withdrawn
945-709 Withdrawn
945-683 Withdrawn
945-769 Withdrawn
945-733 Withdrawn
945-773 Withdrawn
945-686 Withdrawn
945-691 Withdrawn
945-703 Withdrawn
945-716 Withdrawn
945-718 Withdrawn
945-730 Withdrawn
945-679 Withdrawn
945-717 Withdrawn
945-729 Withdrawn
945-689 Withdrawn
945-768 Withdrawn
945-687 Withdrawn
945-724 Withdrawn
945-705 Withdrawn
945-693 Withdrawn
945-732 Withdrawn
945-734 Withdrawn
945-771 Withdrawn
945-688 Withdrawn

Same Product Code

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GEM Premier 7000 with iQM3 PAK (BG/ISE/GL/COOX/Tbili 450 Tests) Instrumentation Laboratory SPA 5
Nova Nova Biomedical Corporation 4
GEM Premier 7000 with iQM3 PAK (BG/ISE/COOX/Tbili 150 Tests) Instrumentation Laboratory SPA 4
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Showing 12 of 235. All products under Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K160153 2016-11-04
K142898 2015-06-17
K131988 2013-09-17
K130144 2013-07-31
K123748 2013-05-07
K122729 2012-11-16
K122642 2012-10-26
K120197 2012-03-19
K111897 2011-07-19
K110416 2011-03-24
K100777 2010-12-10
K043218 2005-05-10
K041874 2004-10-08

Recalls

14 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2025-03-21 Class II Component design/selection ABL90 FLEX and ABL90 FLEX PLUS analyzers running with Radiometer Windows 10 versions RWIN10 1.0 and RWIN10 1.1 may unexpectedly freeze (the analyzer ceases to operate) during a sample measurement. The analyzer software includes a feature (w 6275 analyzers
2024-05-31 Class II Nonconforming Material/Component Issue with analyzer when the pH of the calibration solution decreases during the in-use period potentially because of bacterial growth in the calibration solution bottles. This may result in a probability of reporting biased out-of-specifi 27,127 analyzers
2022-05-18 Class II Software design There is a potential for sporadic incidents of positive and negative biases for analyzer systems configured with cNa+, cCa+, and cK+. 1489 analyzers
2021-04-14 Class II Device Design Due to an issue with the internal clock of the analyzers with an e3800 PC unit installed. Total=4,135 analyzers world-wide (only 1277 analyzers within
2020-05-26 Class II Software design Potential risk of patient mix-up on analyzers due to software issues. 3,899 units 2023-02-08
2020-05-26 Class II Software design Potential risk of patient mix-up on analyzers due to software issues. 4,615 units 2023-02-08
2020-05-11 Class II Under Investigation by firm Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood gases, electrolytes, glucose, lactate, hematocrit and oximetry may misinterpret the contents of some barcode types not using a check digit for patient ID or accessi 1981 2023-02-24
2020-05-11 Class II Under Investigation by firm Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood gases, electrolytes, glucose, lactate, hematocrit and oximetry may misinterpret the contents of some barcode types not using a check digit for patient ID or accessi 9373 units 2023-02-24
2020-03-10 Class II Software design Analyzer’s barcode reader misinterprets the contents of barcode label used for entering patient ID or accession number. The issue is related to barcode types not using a check digit. This could result in patient mixup or loss of sample res 3,656 units 2022-10-31
2020-03-06 Class II Component design/selection Through internal investigation is has been determined that an incorrect component was used within the power supply. The incorrect component may cause a short circuit within the power supply resulting in a delay in treatment. The delay could 2 units
2020-02-03 Class II Software design The firm received reports of occurrences where the barcode reader misinterpreted the contents of a locally printed barcode label used for entering patient ID or accession number into the analyzer in connection with a sample measurement. T 3,968 units 2022-09-20
2019-11-21 Class II Nonconforming Material/Component The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer cuvettes, a subcomponent of the optical system which measures ctHb and derivates. In a cuvette with light shunt, some of the received light has not been transmitted 544 2024-11-08
2019-11-21 Class II Nonconforming Material/Component The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer cuvettes, a subcomponent of the optical system which measures ctHb and derivates. In a cuvette with light shunt, some of the received light has not been transmitted 1233 units 2024-11-08
2018-02-27 Class II Device Design There is a potential problem relating to the AQURE System, versions 2.3.0 and 2.3.1, that may result in patient mix-up. 2 2019-03-20

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer