ACE

ALT Reagent

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code CKA
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70

Record

Regulatory record for ACE
Listed by Alfa Wassermann, United States
FDA product code CKA
Device type Nadh Oxidation/Nad Reduction, Alt/Sgpt
Device class Class 1
Regulation 21 CFR 862.1030
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K113382
Record published 2017-10-10
Record revised 2018-07-06 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for ACE
Catalogue number Size Status
SA1046 In distribution
SA1052 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biobase Biobase Biodustry(Shandong)Co., Ltd. 18
Alanine Aminotransferase (ALT) Randox Laboratories Limited 10
Synermed® Infrared Laboratory Systems LLC 7
JAS Diagnostics Drew Scientific, Ltd. 6
Carolina Liquid Chemistries Corp.® Alanine Aminotransferase Reagent KIT ST240 Carolina Liquid Chemistries 4
Synchron Beckman Coulter, Inc. 4
Architect Abbott Ireland 4
Architect Abbott Medical 3
Alinity Abbott Ireland 3
Pointe Scientific ALT (Sgpt) Liquid Horiba Instruments Incorporated 3
Architect Abbott Laboratories 3
Vitros Ortho-Clinical Diagnostics, Inc. 3

Showing 12 of 57. All products under Nadh Oxidation/Nad Reduction, Alt/Sgpt

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K113382 2012-07-19

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 Closed
2014-03-05 Class II Process control Extremely low absorbance readings. 731 Kits 2015-08-13

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