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Lh

FDA UDI

Class I (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
LH FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The DRG:Hybrid-XL LH is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of luteinizing hormone in serum and plasma. FDA UDI
Model / Reference
HYE-5362 FDA UDI
Description
The DRG:Hybrid-XL LH is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of luteinizing hormone in serum and plasma. FDA UDI

Identifiers

Catalog Number
HYE-5362 FDA UDI
Primary DI / UDI-DI
00840239053626 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

Yes

FDA UDI

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

Lh by DRG International, 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

Sources (1)

  • FDA UDI 0a3d95d8-08b7-43f4-9967-a98b6caf2de0 36 fields · synced May 30, 2026