Identity
- Trade Name
- Freeze Away Dual Action 8ct FDA UDI
- Generic Name
- Wart-removal cryogenic kit FDA UDI
- Device Name
- Combination Cryogenic and Liquid Wart Remover FDA UDI
- Model / Reference
- 90000336 FDA UDI
- Description
- Combination Cryogenic and Liquid Wart Remover FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10888853002955 FDA UDI
- FDA Product Code
- GEH FDA UDI
- GMDN Term
- Wart-removal cryogenic kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4350 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
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Wart-removal cryogenic kit
Freeze Away Dual Action 8ct by Scholl's Wellness Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Scholl's Wellness Company
Sources (1)
- FDA UDI 8ec3cc74-1763-4871-bad1-68986521ab6a 35 fields · synced Jun 8, 2026