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Teco Diagnostics Cholesterol (Liquid) Reagent Set

FDA UDI

Class I (US FDA UDI)

by Teco Diagnostics

Identity

Trade Name
Teco Diagnostics Cholesterol (Liquid) Reagent Set FDA UDI
Generic Name
Total cholesterol lipid IVD, reagent FDA UDI
Device Name
Teco Diagnostics Cholesterol (Liquid) Reagent Set is used for the quantitative determination of total cholesterol in serum. FDA UDI
Model / Reference
C507-100 FDA UDI
Description
Teco Diagnostics Cholesterol (Liquid) Reagent Set is used for the quantitative determination of total cholesterol in serum. FDA UDI

Identifiers

Catalog Number
C507-100 FDA UDI
Primary DI / UDI-DI
10673486001402 FDA UDI
510(k) Number
K914160 FDA UDI
FDA Product Code
CHH FDA UDI
GMDN Term
Total cholesterol lipid IVD, reagent 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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, reagent

Teco Diagnostics Cholesterol (Liquid) Reagent Set by Teco Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total cholesterol lipid IVD, reagent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teco Diagnostics

Sources (1)

  • FDA UDI c955147c-096b-4ab6-96f7-a1377cb34e72 37 fields · synced Jun 6, 2026