Identity
- Trade Name
- MICROPOWER FDA UDI
- Generic Name
- Multi-purpose surgical power tool system, line-powered FDA UDI
- Device Name
- MICROPOWER MEDIUM SPEED DRILL, PERMANENT LEVER FDA UDI
- Model / Reference
- 6021-021 FDA UDI
- Description
- MICROPOWER MEDIUM SPEED DRILL, PERMANENT LEVER FDA UDI
Identifiers
- Catalog Number
- 6021-021 FDA UDI
- Primary DI / UDI-DI
- 20845854013189 FDA UDI
- 510(k) Number
- K072706 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Multi-purpose surgical power tool system, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Micropower 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 0649f376-e160-4cc8-bc3c-8c7dbdfb1899 37 fields · synced May 30, 2026