Identity
- Trade Name
- Nuaskin Skin Tag Remover FDA UDI
- Generic Name
- Scarifier FDA UDI
- Device Name
- For use on: Skin Vegetations Fatty Grains Freckles Age Spots Warts Verruca Large Moles Large Freckles FDA UDI
- Model / Reference
- FY-111 FDA UDI
- Description
- For use on: Skin Vegetations Fatty Grains Freckles Age Spots Warts Verruca Large Moles Large Freckles FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860003125588 FDA UDI
- FDA Product Code
- MIJ FDA UDI
- GMDN Term
- Scarifier FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Scarifier
Nuaskin Skin Tag Remover by Home Aide Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Home Aide Diagnostics, Inc.
Sources (1)
- FDA UDI de7e31a0-f6d0-4c78-bfaf-d9f5a0a4e984 34 fields · synced May 30, 2026