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Wondfo

FDA UDI

Class II (US FDA UDI)

by Wondfo Usa Co., Ltd.

Identity

Trade Name
Wondfo FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
1-Midstream DoCheck Wide Tip;1 per box;hCG Pregnancy Test 25 mIU/mL OTC FDA UDI
Model / Reference
DW1-M-DW FDA UDI
Description
1-Midstream DoCheck Wide Tip;1 per box;hCG Pregnancy Test 25 mIU/mL OTC FDA UDI

Identifiers

Primary DI / UDI-DI
00816862024326 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 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

No

FDA UDI

Convenience Kit

No

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: Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

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

Similar devices

Also classified as Total human chorionic gonadotropin 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 1aa70c67-c554-48f7-98a5-27d5113884c9 35 fields · synced Jun 8, 2026