Identity
- Trade Name
- POWERPRO FDA UDI
- Generic Name
- Drilling power tool attachment, basic FDA UDI
- Device Name
- POWERPRO HIGH SPEED DRILL ATTACHMENT FDA UDI
- Model / Reference
- PRO2033 FDA UDI
- Description
- POWERPRO HIGH SPEED DRILL ATTACHMENT FDA UDI
Identifiers
- Catalog Number
- PRO2033 FDA UDI
- Primary DI / UDI-DI
- 20845854028381 FDA UDI
- FDA Product Code
- DZI FDA UDI
- GMDN Term
- Drilling power tool attachment, basic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.4120 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Powerpro by Conmed Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI d8a01021-0337-4dd7-8b94-ef5160dc0bc0 36 fields · synced May 31, 2026