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Teco Diagnostics Lipase Reagent Set

FDA UDI

Class I (US FDA UDI)

by Teco Diagnostics

Identity

Trade Name
Teco Diagnostics Lipase Reagent Set FDA UDI
Generic Name
Lipase IVD, reagent FDA UDI
Device Name
Teco Diagnostics Lipase Reagent Set is used for the quantitative turbidimetric determination of pancreatic lipase in human serum. FDA UDI
Model / Reference
L537-100 FDA UDI
Description
Teco Diagnostics Lipase Reagent Set is used for the quantitative turbidimetric determination of pancreatic lipase in human serum. FDA UDI

Identifiers

Catalog Number
L537-100 FDA UDI
Primary DI / UDI-DI
10673486002089 FDA UDI
510(k) Number
K915706 FDA UDI
FDA Product Code
CET FDA UDI
GMDN Term
Lipase IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1465 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: Lipase IVD, reagent

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

Similar devices

Also classified as Lipase IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teco Diagnostics

Sources (1)

  • FDA UDI 957e059f-ad1c-475d-bbf3-c340b1cdd4d2 37 fields · synced May 30, 2026