Synchron

Enzymatic Creatinine Reagent (CR-E 2 x 200)

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code
2recalls on this code

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 Synchron
Listed by Beckman Coulter, Inc., United States
FDA product code JFY
Device type Enzymatic Method, Creatinine
Device class Class 2
Regulation 21 CFR 862.1225
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Record published 2016-08-24
Record revised 2023-08-28 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Synchron
Catalogue number Size Status
A60298 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
Creatinine plus ver.2 Roche Diagnostics Gmbh 1
Dimension® Flex® reagent cartridge Ezcr 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
K093458 2009-12-04
K091742 2009-08-14

Recalls

2 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
2019-08-15 Class II Device Design It has been determined that N-acetyl p benzoquinone imine (NAPQI), a metabolite of acetaminophen (paracetamol), may cause negative interference for assays if present in high quantities in serum due to acetaminophen overdoese. This could res 2581 Reagents 2024-02-28
2017-04-03 Class II Under Investigation by firm Beckman Coulter has identified the following drugs as potential sources of interference: Metamizole (Dipyrone), Sulfasalazine, and Sulfapyridine and may result in false low results. 12,665 units total (1,399 units in US) 2018-05-31

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