Catalogue number SK6122-20, listed by Sekisui Diagnostics, LLC, United States, under Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl. 2 manufacturers in China are registered for 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.
Record
Regulatory record for HDL Ultra Cholesterol Reagent | Listed by | Sekisui Diagnostics, LLC, United States |
| 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, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2016-09-20 |
| Record revised | 2026-06-30 (version 5) |
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 |
| Distribution end date | 2021-06-01 |
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.