Carolina Liquid Chemistries Corp.® BUN RGT. KIT AU-252

BUN (Blood Urea Nitrogen) 3 x 300 tests

Registry build 21.09.26
1manufacturer
1catalogue number
1510(k) clearance

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code CDQ
Manufacturer City Province Registered as Device types
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61

Record

Regulatory record for Carolina Liquid Chemistries Corp.® BUN RGT. KIT AU-252
Listed by Carolina Liquid Chemistries, United States
FDA product code CDQ
Device type Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device class Class 2
Regulation 21 CFR 862.1770
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-09-01
Record revised 2023-08-14 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Special storage condition: Unopened Reagent is stable when stored at 2-8° C until expiration date; Storage environment temperature 2 to 8 °C
Sizes Total volume 60 ml

Catalogue Numbers

Catalogue numbers for Carolina Liquid Chemistries Corp.® BUN RGT. KIT AU-252
Catalogue number Size Status
AU-252 Total Volume 60 ml In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
JAS Diagnostics Drew Scientific, Ltd. 12
Urea Randox Laboratories Limited 12
Synermed® Infrared Laboratory Systems LLC 8
Pointe Scientific, Inc. Horiba Instruments Incorporated 6
AU Beckman Coulter, Inc. 6
UreaBUN Roche Diagnostics Gmbh 3
Kinetic UV assay for ureaurea nitrogen Roche Diagnostics Gmbh 3
Pointe Scientific BUN Liquid Horiba Instruments Incorporated 3
Alinity Abbott Medical 2
Architect Abbott Laboratories 2
Architect Abbott Medical 2
Urea Nitrogen (BUN) Liqui-UV® Stanbio Laboratory, L.P. 2

Showing 12 of 49. All products under Urease And Glutamic Dehydrogenase, Urea Nitrogen

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K971967 1997-06-17

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