Wired Barcode Scanner (4k) (3500) (5k)

Catalogue number 00025000420, listed by Instrumentation Laboratory SPA, Italy, under Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
16510(k) clearances naming this product code
35recalls 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 Wired Barcode Scanner (4k) (3500) (5k)
Listed by Instrumentation Laboratory SPA, Italy
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 Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-09-23
Record revised 2021-07-14 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries serial number

Catalogue Numbers

Catalogue numbers for Wired Barcode Scanner (4k) (3500) (5k)
Catalogue number Size Status
00025000420 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stat Profile Nova Biomedical Corporation 80
ABL80 SC80 Radiometer Medical APS 66
ABL77 Sci Radiometer Medical APS 14
Electrode for ABL analyzers Radiometer Medical APS 7
Calibration Solution Radiometer Medical APS 7
i-STAT Abbott Point OF Care Inc. 6
ABL90 Sensor Cassette pack Radiometer Medical APS 6
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
Calibration Gas 2 Radiometer Medical APS 3
Ready Sensor™ Lactate Biosensor Siemens Healthcare Diagnostics Inc 3

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
K223608 2023-08-10
K203790 2021-08-20
K173403 2017-12-29
K160412 2016-12-14
K133407 2014-01-13
K061974 2006-09-15
K992834 1999-11-24
K963800 1996-11-13
K955793 1996-02-14
K935069 1994-03-28
K913927 1991-10-11
K890827 1989-06-20
K821483 1982-06-10
K820744 1982-04-15
K800757 1980-04-21
K760969 1977-01-12

Recalls

31 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
2026-05-21 Class II Nonconforming Material/Component The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing specifications. The malfunction could result in delayed recognition and management of Co-O 32 units
2026-05-21 Class II Nonconforming Material/Component The active ingredient concentration in the lysing bag solution of specific GEM Premier 5000 lots did not meet established manufacturing specifications. The malfunction could result in delayed recognition and management of Co-Oximetry and to 109 units
2026-05-08 Class II Software Design Change BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the “price c 4 US
2026-05-08 Class II Software Design Change BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the “price c 0 US, 118 OUS
2026-05-08 Class II Software Design Change BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the “price c 67
2026-05-08 Class II Software Design Change BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the “price c 27
2026-05-08 Class II Software Design Change BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the “price c 21
2026-05-08 Class II Software Design Change BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the “price c 3
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 489 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 130 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 1,629 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 180 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 27 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 253 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 1,126 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 7 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 70 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 352 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 1,989 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 1,225 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 195 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 1,607 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 25 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 30 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 51 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 74 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 10 units
2026-01-20 Class II Nonconforming Material/Component Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, 8 units
2023-09-29 Class II Under Investigation by firm Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications f 2448 total
2023-09-29 Class II Under Investigation by firm Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications f 2448 units
2023-09-29 Class II Under Investigation by firm Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications f 2448 units
2011-05-11 Not classified Software design Software upgrade: misuse of the barcode gun by repeatedly clicking can cause the instrument to attach test results to an incorrect patient ID. 840 units 2013-03-15
2007-03-27 Not classified Other Instrument in Micro Sampling Mode failed to aspirate and no error code was generated and an incorrect patient report could result 210 2012-05-23
2003-03-07 Not classified Other Incorrect bar code applied to cartridges could result in inaccurate pO2 value 16 2012-05-23
2003-03-07 Not classified Other Incorrect bar code applied to cartridges could result in inaccurate pO2 value 2 2012-05-23

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.

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