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DELFIA hLH Spec kit

FDA UDI

Class I (US FDA UDI)

by Wallac, Inc.

Identity

Trade Name
DELFIA hLH Spec kit FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Time-resolved fluoroimmunoassay for the quantitative determination of human luteinizing hormone (hLH). FDA UDI
Model / Reference
A031-101 FDA UDI
Description
Time-resolved fluoroimmunoassay for the quantitative determination of human luteinizing hormone (hLH). FDA UDI

Identifiers

Catalog Number
A031-101 FDA UDI
Primary DI / UDI-DI
06438147009206 FDA UDI
FDA Product Code
CEP FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1485 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

No

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: Luteinizing hormone (LH) IVD, kit, enzyme immunoassay (EIA)

DELFIA hLH Spec kit by Wallac, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luteinizing hormone (LH) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wallac, Inc.

Sources (1)

  • FDA UDI d5e789b9-ba8d-494a-9706-12583b90944e 35 fields · synced Jun 1, 2026