Cobas B 221 S3 Fluid Pack

Catalogue number 3260933184, listed by Roche Diagnostics Gmbh, Germany, under Acid, Lactic, Enzymatic Method. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Shandong (1), Hunan (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code KHP
Manufacturer City Province Registered as Device types
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70
AVE Science & Technology Co., Ltd. Changsha Hunan Manufacturer 22
Eaglenos Sciences, Inc. Nanjing Jiangsu Manufacturer 4

Record

Regulatory record for cobas b 221 S3 Fluid Pack
Listed by Roche Diagnostics Gmbh, Germany
FDA product code KHP
Device type Acid, Lactic, Enzymatic Method
Device class Class 1
Regulation 21 CFR 862.1450
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Record published 2016-09-20
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 25 °C

Catalogue Numbers

Catalogue numbers for cobas b 221 S3 Fluid Pack
Catalogue number Size Status
3260933184 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
StatSensor/StatStrip Nova Biomedical Corporation 5
Stat Profile Nova Biomedical Corporation 5
Lactate Gen.2 Roche Diagnostics Gmbh 4
Lactate Plus Nova Biomedical Corporation 4
Biobase Biobase Biodustry(Shandong)Co., Ltd. 3
i-STAT Abbott Point OF Care Inc. 3
Alinity Abbott Medical 2
Fora Fora Care Inc. 2
Vitros Ortho-Clinical Diagnostics, Inc. 2
LA Cartridge LifeHealth, LLC 2
L-Lactate (LAC) Randox Laboratories Limited 2
ABX Pentra Lactic Acid Horiba ABX SAS 1

Showing 12 of 43. All products under Acid, Lactic, Enzymatic Method

Recalls

1 of these is 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
2018-12-17 Class II Device Design New endogenous interference claims have been established for the following assays used on the cobas c 311 analyzer and the cobas c 501, 502, 701, 702, and Modular Analytics P/D modules which may have potential medical risk. ***Update: Cobas 5292 analytical units 2020-11-02

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