Identity
- Trade Name
- Cosmopen FDA UDI
- Generic Name
- Dermabrasion brush, rotary FDA UDI
- Model / Reference
- Cosmopen Tips -Type A FDA UDI
Identifiers
- Catalog Number
- CPMNT030 FDA UDI
- Primary DI / UDI-DI
- G589CPMNT030 FDA UDI
- FDA Product Code
- GFE FDA UDI
- GMDN Term
- Dermabrasion brush, rotary FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Combination Product
Yes
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
Radiation Sterilization FDA UDI
Category: Dermabrasion brush, rotary
Cosmopen by CosmoFrance — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- CosmoFrance
Sources (1)
- FDA UDI 1fec4625-7a60-4e52-9268-0f18f6d7f323 33 fields · synced May 29, 2026