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Proov

FDA UDI

Class II (US FDA UDI)

by Mfb Fertility, Inc.

Identity

Trade Name
Proov FDA UDI
Generic Name
Natural conception assistance kit FDA UDI
Device Name
At home fertility test that measures all 4 cycle hormones for a comprehensive fertility map. FDA UDI
Model / Reference
Pregnancy Pack FDA UDI
Description
At home fertility test that measures all 4 cycle hormones for a comprehensive fertility map. FDA UDI

Identifiers

Primary DI / UDI-DI
00850035206126 FDA UDI
FDA Product Code
JHI FDA UDI
LCX FDA UDI
QKE FDA UDI
NGE FDA UDI
GMDN Term
Natural conception assistance kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 FDA UDI
862.1620 FDA UDI
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Natural conception assistance kit

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

Similar devices

Also classified as Natural conception assistance kit.

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 ebf45ccf-0cba-4a57-8462-b9ac598f386f 33 fields · synced May 30, 2026