Cobas Infinity POC IT Solutions

Catalogue number 08739170001, listed by Roche Diagnostics Gmbh, Germany, under Calculator/Data Processing Module, For Clinical Use. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
1catalogue number
11recalls on this code

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JQP
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Gene Science Co., Ltd. Shaoxing Zhejiang Manufacturer 31
Foshan Zike Technology Co., Ltd. Foshan Guangdong Manufacturer 9
Tianjin Empecs Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 8
Shanghai Bestcovered Limited Shanghai Shanghai Manufacturer 2

Record

Regulatory record for cobas infinity POC IT solutions
Listed by Roche Diagnostics Gmbh, Germany
FDA product code JQP
Device type Calculator/Data Processing Module, For Clinical Use
Device class Class 1
Regulation 21 CFR 862.2100
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-12-21
Record revised 2024-03-15 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number
Distribution end date 2021-09-22

Catalogue Numbers

Catalogue numbers for cobas infinity POC IT solutions
Catalogue number Size Status
08739170001 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SoftPathDx SCC Soft Computer 69
SoftMolecular SCC Soft Computer 67
SoftFlowCytometry SCC Soft Computer 67
SoftBiochemistry SCC Soft Computer 67
SoftCytogenetics SCC Soft Computer 67
SoftMic SCC Soft Computer 65
SoftLab SCC Soft Computer 64
SoftTrack SCC Soft Computer 61
SoftHLA SCC Soft Computer 61
SoftGenomics SCC Soft Computer 51
SoftGenePortal SCC Soft Computer 48
SoftTotalQC SCC Soft Computer 28

Showing 12 of 140. All products under Calculator/Data Processing Module, For Clinical Use

Recalls

6 of these are Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2019-04-04 Class III Nonconforming Material/Component There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument. 4 units 2020-05-12
2019-04-04 Class III Nonconforming Material/Component There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument. 9 units 2020-05-12
2019-02-04 Class II Software design Using the following versions of cobas infinity software (2.0 thorough 2.5), there is a potential where the results from the first sample subsequent to the bottle change, (when using the Standby bottle function), does not display a quality c 15 units 2020-09-16
2018-07-16 Class II Under Investigation by firm Sample material may potentially come in contact with the pipetting nozzle during operation of cobas p 612 pre-analytical system (63x) (LCP1) with non-filter tips. The possible presence of biological material on the nozzle may cause contamin 12 units 2019-05-16
2017-05-09 Class II Device Design a gap between the conveyor belt and the rack tray table (plastic part) may cause vibration of the 5 position racks during the transport. This issue can pose a
potential risk to involved operators and can also lead to potential cross contami
3 2018-02-02
2017-03-01 Class II Under Investigation by firm Roche Diagnostics Corp. initiated a voluntary correction because a rack crash may occur on the Cobas 8100 bi-directional reformatter (BRF) and uni-directional
reformatter (BRF) modules with software version 02-xx, only when rack buffering i
45 2018-07-03
2017-03-01 Class II Under Investigation by firm “Roche Diagnostics Corp. initiated a voluntary correction because a rack crash may occur on the Cobas 8100 bi-directional reformatter (BRF) and uni-directional
reformatter (URF) modules with software version 02-xx, only when rack buffering
45 Units 2018-07-03
2016-12-27 Class II Software design 5 2017-08-04
2009-04-01 Not classified Component design/selection Some data alarm flags do not transfer from the analyzer to the laboratory information system, since not all data flags are recognized by the instrument manager/middleware. 498 of all products 2009-12-07
2009-04-01 Not classified Component design/selection Some data alarm flags do not transfer from the analyzer to the laboratory information system, since not all data flags are recognized by the instrument manager/middleware. 498 of all products. 2009-12-07
2003-06-26 Not classified Other A software bug in version 3.0 may result in prolonged mixing time, evaporation of elution volume and biased sample results for various protocols. 17 2003-11-19

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