ExtendSURE

The lypholised Hemoglobin A1c Linearity controls are prepared from human blood and contain normal hemoglobin, preservatives and stabilizers. The controls are formulated to give enhanced…

Registry build 21.09.26

The lypholised Hemoglobin A1c Linearity controls are prepared from human blood and contain normal hemoglobin, preservatives and stabilizers. The controls are formulated to give enhanced stability. The Lyophilized Hemoglobin A1c Linearity Controls are intended to verify the linearity of HbA1c assays across the patient reportable range (4 to 18%, NGSP aligned) using protocols setup within individual clinical laboratories.

12manufacturers in China registered for this device type
5catalogue numbers in this listing
2510(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 ExtendSURE
Listed by Canterbury Scientific Ltd., New Zealand
FDA product code JJX
Device type Single (Specified) Analyte Controls (Assayed And Unassayed)
Device class Class 1
Regulation 21 CFR 862.1660
Establishment Manufacturer
Premarket notification Exempt
Record published 2018-09-20
Record revised 2019-07-24 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature 2 to 8 °C
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for ExtendSURE
Catalogue number Size Status
B12397 In distribution
HB710SBAr In distribution
B12396 In distribution
107253 In distribution
HB510 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
K071648 2007-08-22
K043070 2004-12-09

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