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Cholesterol LiquiColor®

FDA UDI

Class I (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
Cholesterol LiquiColor® FDA UDI
Generic Name
Total cholesterol lipid IVD, kit, spectrophotometry FDA UDI
Device Name
For the Quantitative-Enzymatic-Colorimetric Determination of Total and HDL Cholesterol in Serum or Plasma. FDA UDI
Model / Reference
1010-430 FDA UDI
Description
For the Quantitative-Enzymatic-Colorimetric Determination of Total and HDL Cholesterol in Serum or Plasma. FDA UDI

Identifiers

Catalog Number
1010-430 FDA UDI
Primary DI / UDI-DI
00657498000649 FDA UDI
FDA Product Code
CHH FDA UDI
GMDN Term
Total cholesterol lipid IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total cholesterol lipid IVD, kit, spectrophotometry

Cholesterol LiquiColor® by Stanbio Laboratory, L.p. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total cholesterol lipid IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f788c29-88b6-4676-9d84-c480aa6c8134 36 fields · synced Jun 1, 2026