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HORMONElife™

FDA UDI

Class I (US FDA UDI)

by Wondfo Usa Co., Ltd.

Identity

Trade Name
HORMONElife™ FDA UDI
Generic Name
Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
HORMONElife™ Ultra Accurate FSH Test Strip OTC 6PK FDA UDI
Model / Reference
W52-S-SQ-6BX FDA UDI
Description
HORMONElife™ Ultra Accurate FSH Test Strip OTC 6PK FDA UDI

Identifiers

Primary DI / UDI-DI
00816862027242 FDA UDI
FDA Product Code
NGA FDA UDI
GMDN Term
Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1300 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: Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing

HORMONElife™ by Wondfo Usa Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 356154ba-16c6-4790-bdc5-1be0853026d8 34 fields · synced May 30, 2026