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, 1 Test per Kitbox with Holder FDA UDI
- Model / Reference
- WCOVFLU-OTC-1 FDA UDI
- Description
- WELLlife™ COVID-19/Flu A&B Home Test Cassette, 1 Test per Kitbox with Holder FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00816862026887 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
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: 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.
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- BinaxNOW COVID-19/Flu A&B Combo Self Test — Alere Scarborough, Inc. · Class II
- BinaxNOW COVID-19/Flu A&B Combo Self Test — Alere Scarborough, Inc. · Class II
- Healgen — Healgen Scientific Limited Liability Company · Class II
- BinaxNOW COVID-19/Flu A&B Combo Self Test — Alere Scarborough, Inc. · Class II
- GenaCheck® COVID-19/Flu A&B Rapid Self-Test — Genabio Diagnostics Inc. · Class II
- Rapid Response — BTNX Inc · Class II
- BinaxNOW COVID-19/Flu A&B Combo Self Test — Alere Scarborough, Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Wondfo Usa Co., Ltd.
Sources (1)
- FDA UDI 9aae10f8-5551-4a32-917a-390d1cd8ff3a 35 fields · synced May 30, 2026