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Luteinizing Hormone (LH) ELISA

FDA UDI

Class I (US FDA UDI)

by American Laboratory Products Company

Identity

Trade Name
Luteinizing Hormone (LH) ELISA FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Intended for the direct quantitative determination of Luteinizing Hormone by an enzyme immunoassay in human serum. For in vitro diagnostic use. FDA UDI
Model / Reference
11-LUTHU-E01 FDA UDI
Description
Intended for the direct quantitative determination of Luteinizing Hormone by an enzyme immunoassay in human serum. For in vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
11-LUTHU-E01 FDA UDI
Primary DI / UDI-DI
B24211LUTHUE010 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

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

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

Luteinizing Hormone (LH) ELISA by American Laboratory Products Company — 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

Sources (1)

  • FDA UDI 5d410996-bf36-4490-af00-1012a055dbc9 36 fields · synced May 30, 2026