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Proov

FDA UDI

Class I (US FDA UDI)

by Mfb Fertility, Inc.

Identity

Trade Name
Proov FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
At home IVD LH tests (also called ovulation tests or OPKs) measure luteinizing hormone before ovulation to identify your two most fertile days. FDA UDI
Model / Reference
Predict FDA UDI
Description
At home IVD LH tests (also called ovulation tests or OPKs) measure luteinizing hormone before ovulation to identify your two most fertile days. FDA UDI

Identifiers

Primary DI / UDI-DI
00850035206102 FDA UDI
FDA Product Code
NGE FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing 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

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, rapid ICT, self-testing

Proov by Mfb Fertility, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mfb Fertility, Inc.

Sources (1)

  • FDA UDI d83d5ebb-0e9c-4c18-9738-4ad5b9bc1dd6 33 fields · synced Jun 8, 2026