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Clinical Guard

FDA UDI

Class I (US FDA UDI)

by Clinical Guard

Identity

Trade Name
Clinical Guard FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
Ovulation Urine Test Strip Pack of 50 FDA UDI

Identifiers

Primary DI / UDI-DI
00897429002766 FDA UDI
FDA Product Code
NGE FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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, rapid ICT, clinical

Clinical Guard by Clinical Guard — Class I — 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

Manufacturer
Clinical Guard

Sources (1)

  • FDA UDI 148c8c4e-c35f-4db9-97d3-cbb8eb4711c2 32 fields · synced May 30, 2026