AST

The AST method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of aspartate aminotransferase activity in serum or…

Registry build 21.09.26

The AST method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of aspartate aminotransferase activity in serum or plasma.

2manufacturers in China registered for this device type
10catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

Concentrated in Jilin (1), Shandong (1).

Chinese manufacturers registered for FDA product code CIT
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70

Record

Regulatory record for AST
Listed by Randox Laboratories Limited, United Kingdom
FDA product code CIT
Device type Nadh Oxidation/Nad Reduction, Ast/Sgot
Device class Class 2
Regulation 21 CFR 862.1100
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer
510(k) K923505
Record published 2016-09-09
Record revised 2025-05-12 (version 4)

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
Storage Storage environment temperature 2 to 8 °C
Distribution end date 2016-09-16

Catalogue Numbers

Catalogue numbers for AST
Catalogue number Size Status
AS2800 In distribution
AS1267 In distribution
AS8306 In distribution
AS1204 In distribution
AS1202 In distribution
AS7938 In distribution
AS2359 In distribution
AS3876 In distribution
AS3804 In distribution
AS7905 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biobase Biobase Biodustry(Shandong)Co., Ltd. 19
JAS Diagnostics Drew Scientific, Ltd. 7
Synermed® Infrared Laboratory Systems LLC 7
Pointe Scientific, Inc. Horiba Instruments Incorporated 5
AU Beckman Coulter, Inc. 4
Architect Abbott Ireland 4
Synchron Beckman Coulter, Inc. 4
ACE Alfa Wassermann 4
Architect Abbott Medical 3
Alinity Abbott Ireland 3
Architect Abbott Laboratories 3
Aspartate aminotransferase acc to Ifcc withwithout pyridoxal phosphate activat Roche Diagnostics Gmbh 3

Showing 12 of 62. All products under Nadh Oxidation/Nad Reduction, Ast/Sgot

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K923505 1992-11-16

Recalls

1 of these is 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
2023-09-06 Class II Under Investigation by firm RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i
issues with the re-run feature conditions when inco
6 units

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