Identity

Trade Name
Healgen FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI
Device Name
LH Ovulation Rapid Test Midstream(Urine,40mIU/mL) FDA UDI
Model / Reference
GALH-103b FDA UDI
Description
LH Ovulation Rapid Test Midstream(Urine,40mIU/mL) FDA UDI

Identifiers

Catalog Number
GALH-103b FDA UDI
Primary DI / UDI-DI
00816490021056 FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI

Classification

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

Yes

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, rapid ICT, clinical

Healgen by Healgen Scientific Limited Liability Company — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 34468717-0628-4803-bb90-9e0da1905d7c 36 fields · synced Jun 8, 2026