Identity
- Trade Name
- MD 30 FDA UDI
- Generic Name
- Remotely-driven dental drilling system motor FDA UDI
- Device Name
- Dental implant motor system, SET FDA UDI
- Model / Reference
- 2005CAM FDA UDI
- Description
- Dental implant motor system, SET FDA UDI
Identifiers
- Primary DI / UDI-DI
- ENOU2005CAM0 FDA UDI
- 510(k) Number
- K042434 FDA UDI
- FDA Product Code
- DZI FDA UDI
- GMDN Term
- Remotely-driven dental drilling system motor 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
Md 30 by Nouvag AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Nouvag AG
Sources (1)
- FDA UDI e3aadfe7-fbd5-4e29-bd89-9211478bb100 36 fields · synced May 30, 2026