D-10

D-10 Hemoglobin A1c Program Calibrator/Diluent Set

Registry build 21.09.26
2manufacturers in China registered for this device type
3catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

All of them in Shanghai.

Chinese manufacturers registered for FDA product code PDJ
Manufacturer City Province Registered as Device types
Shanghai Medconn Medical Technology Co., Ltd. Shanghai Shanghai Manufacturer 2
Shanghai Medconn Biotechnology Co., Ltd. Jinshan District Shanghai Manufacturer 2

Record

Regulatory record for D-10
Listed by Bio-Rad Laboratories Inc., United States
FDA product code PDJ
Device type Hemoglobin A1c Test System
Device class Class 2
Regulation 21 CFR 862.1373
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2017-07-21
Record revised 2023-06-05 (version 7)

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

Catalogue Numbers

Catalogue numbers for D-10
Catalogue number Size Status
12000949 In distribution
12005707 In distribution
12005706 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
D-100 Bio-Rad Laboratories Inc. 4
Architect Abbott Medical 3
Afinion HbA1c Dx Abbott Diagnostics Technologies AS 2
Tina-quant Hemoglobin A1cDx Gen.3 Roche Diagnostics Gmbh 2
Alinity Abbott Medical 1
HbA1c Assay Sekisui Diagnostics, LLC 1
Dimension Vista System Flex reagent cartridge A1C KIT Siemens Healthcare Diagnostics Inc 1
Eluent 80B Arkray USA, Inc. 1
BioHermes Automated Glycohemoglobin Analyzer Wuxi Biohermes BIO & Medical Technology Co., Ltd. 1
Diluent 80 Arkray USA, Inc. 1
Eluent 80A Arkray USA, Inc. 1
Hemolysis Washing Solution 80H Arkray USA, Inc. 1

Showing 12 of 18. All products under Hemoglobin A1c Test System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K161687 2016-10-14
K151321 2015-12-09
K142448 2015-03-24

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