HDL

An HDL-cholesterol test system is a device intended for the quantitative in vitro determination of HDL-cholesterol concentration in human serum and plasma.

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (1), Hebei (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LBS
Manufacturer City Province Registered as Device types
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Shijiazhuang Hipro Biotechnology Co., Ltd. Shijiazhuang Hebei Manufacturer 22

Record

Regulatory record for HDL
Listed by Randox Laboratories Limited, United Kingdom
FDA product code LBS
Device type Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Device class Class 1
Regulation 21 CFR 862.1475
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer
510(k) K982341
Record published 2018-12-24
Record revised 2023-07-06 (version 2)

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 Special storage condition: Store protected from light; Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for HDL
Catalogue number Size Status
CH3811 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
JAS Diagnostics Drew Scientific, Ltd. 6
Direct HDL-Cholesterol (HDL) Randox Laboratories Limited 4
Synermed® Infrared Laboratory Systems LLC 4
AU Beckman Coulter, Inc. 4
HDL-Cholesterol Gen.4 Roche Diagnostics Gmbh 4
Direct HDL Cholesterol LiquiColor® Stanbio Laboratory, L.P. 3
Ultra N-geneous HDL Cholesterol Reagent Sekisui Diagnostics, LLC 2
Advia® Chemistry D-HDL Direct HDL Cholesterol Reagents Siemens Healthcare Diagnostics Inc 2
Vitros Ortho-Clinical Diagnostics, Inc. 2
Alinity Abbott Medical 2
ox-LDL Elisa Immundiagnostik, Inc. 2
ACE Alfa Wassermann 2

Showing 12 of 30. All products under Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K153435 2016-01-08
K982341 1998-07-30
K970735 1997-06-06

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of HDL
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Siemens Healthcare Diagnostics Inc 510(k) number 2016-03-17 Class II Device Design Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC) and Metamizole (Dipyrone) interference with Trinder and Trinder-like reaction assays. Siemens has confirmed that falsely depressed results may occur on samples drawn 137422 units total 2017-09-25

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