Creatinine Plus Ver.2

Catalogue number 08057524190, listed by Roche Diagnostics Gmbh, Germany, under Enzymatic Method, Creatinine. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Zhejiang (1), Guangxi (1), Chongqing (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 JFY
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Urit Medical Electronic Co., Ltd. Guilin Guangxi Contract manufacturer 28
Chong Qing Teco Huayi Pharm. Co. Shapingba Dist. Chongqing Contract manufacturer 18

Record

Regulatory record for Creatinine plus ver.2
Listed by Roche Diagnostics Gmbh, Germany
FDA product code JFY
Device type Enzymatic Method, Creatinine
Device class Class 2
Regulation 21 CFR 862.1225
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K024098
Record published 2020-03-05
Record revised 2025-10-27 (version 3)

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 8 °C

Catalogue Numbers

Catalogue numbers for Creatinine plus ver.2
Catalogue number Size Status
08057524190 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Creatinine Plus Roche Diagnostics Gmbh 3
Teco Diagnostics Teco Diagnostics 3
Pointe Scientific, Inc. Horiba Instruments Incorporated 3
Creatinine plus ver2 Roche Diagnostics Gmbh 3
Architect Abbott Laboratories 2
CR Cartridge LifeHealth, LLC 2
Alinity Abbott Laboratories 2
Creatinine LiquiColor® Stanbio Laboratory, L.P. 2
Pointe Scientific, Inc. Creatinine Enzymatic Horiba Instruments Incorporated 2
Automatic Urine Analyzer Urit Medical Electronic Co., Ltd. 2
Dimension® Flex® reagent cartridge Ezcr Siemens Healthcare Diagnostics Inc 1
Clinitek® Microalbumin 2 Reagent Strips Siemens Healthcare Diagnostics Inc 1

Showing 12 of 40. All products under Enzymatic Method, Creatinine

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K024098 2002-12-19
K003261 2000-11-16

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Creatinine plus ver.2
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Roche Diagnostics Gmbh 510(k) number 2008-06-11 Not classified Labeling Change Control Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader. 1068 2009-09-22

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