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Teco Diagnostics Total Lipid Reagent Set

FDA UDI

Class I (US FDA UDI)

by Teco Diagnostics

Identity

Trade Name
Teco Diagnostics Total Lipid Reagent Set FDA UDI
Generic Name
Total lipoprotein IVD, reagent FDA UDI
Device Name
Teco Diagnostics Total Lipid Reagent Set is used for the quantitative determination of the total lipid index in serum using the sulfo-phospho-vanillin colorimetric method. FDA UDI
Model / Reference
T526-480 FDA UDI
Description
Teco Diagnostics Total Lipid Reagent Set is used for the quantitative determination of the total lipid index in serum using the sulfo-phospho-vanillin colorimetric method. FDA UDI

Identifiers

Catalog Number
T526-480 FDA UDI
Primary DI / UDI-DI
10673486002195 FDA UDI
FDA Product Code
CFD FDA UDI
GMDN Term
Total lipoprotein IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1470 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

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 lipoprotein IVD, reagent

Teco Diagnostics Total Lipid Reagent Set by Teco Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teco Diagnostics

Sources (1)

  • FDA UDI 9e3423b8-9192-4a38-86e5-3ca8eb803ecd 36 fields · synced May 29, 2026