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WELLlife™

FDA UDI

Class II (US FDA UDI)

by Wondfo Usa Co., Ltd.

Identity

Trade Name
WELLlife™ FDA UDI
Generic Name
Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
WELLlife™ COVID-19/Flu A&B Home Test Cassette, 25 Tests per Kitbox FDA UDI
Model / Reference
WFLUAB-OTC-25 FDA UDI
Description
WELLlife™ COVID-19/Flu A&B Home Test Cassette, 25 Tests per Kitbox FDA UDI

Identifiers

Primary DI / UDI-DI
00816862027648 FDA UDI
FDA Product Code
SCA FDA UDI
GMDN Term
Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3987 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

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: Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing

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

Similar devices

Also classified as Multiple-genus respiratory virus antigen 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 9c1032f1-28fe-4b26-9e9f-e18da0941bb0 35 fields · synced Jun 8, 2026