Diabetes Cntl, Bi-L

Diabetes Control BI-Level

Registry build 21.09.26
12manufacturers in China registered for this device type
1catalogue number
8510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (3), Guangdong (3), Jilin (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JJX
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21
Guangdong Transtek Medical Electronics Co., Ltd. Zhongshan Guangdong Contract manufacturer 11
Tianjin Empecs Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 8
BD Rapid Diagnostics (Suzhou) Co., Ltd. China (Jiangsu) Pilot Free Trade Zone Suzhou Area Manufacturer 6
Sejoy Biomedical Co., Ltd. Hangzhou Zhejiang Manufacturer 5
Beijing Genesee Biotech, Inc. Beijing Beijing Manufacturer 4
Human Metabolomics Institute, Inc. Shenzhen Guangdong Manufacturer 4
Changsha Sinocare Inc. Changsha Hunan Manufacturer 2

Record

Regulatory record for Diabetes Cntl, Bi-L
Listed by Cliniqa Corporation, United States
FDA product code JJX
Device type Single (Specified) Analyte Controls (Assayed And Unassayed)
Device class Class 1
Regulation 21 CFR 862.1660
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
510(k) K060570
Record published 2018-08-22
Record revised 2019-02-04 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied as a kit Yes
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Diabetes Cntl, Bi-L
Catalogue number Size Status
91815 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vitros Ortho-Clinical Diagnostics, Inc. 55
Validate LGC Clinical Diagnostics, Inc. 37
Architect Abbott Laboratories 24
Architect Abbott Medical 23
BioPlex 2200 Bio-Rad Laboratories Inc. 22
Architect Abbott Ireland 18
Liquichek Bio-Rad Laboratories Inc. 17
Alinity Abbott Medical 17
Alinity Abbott Ireland 15
Fora Fora Care Inc. 15
Pregnancy-Skreen Biochemical Diagnostics, Inc. 14
Accurun® LGC Clinical Diagnostics, Inc. 14

Showing 12 of 907. All products under Single (Specified) Analyte Controls (Assayed And Unassayed)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121237 2012-05-18
K052679 2005-11-18
K041898 2004-08-16
K040927 2004-05-17
K040455 2004-03-05
K022758 2002-09-17
K022491 2002-08-27
K022232 2002-08-01

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