Identity
- Trade Name
- SET PROIMPLANT 3RD GEN CA 20:1 L FDA UDI
- Generic Name
- Surgical power tool system control unit, line-powered FDA UDI
- Device Name
- Sets of Proimplant systems and their dental micromotors or contra-angles plus relevant accessories FDA UDI
- Model / Reference
- 1700768-001 FDA UDI
- Description
- Sets of Proimplant systems and their dental micromotors or contra-angles plus relevant accessories FDA UDI
Identifiers
- Catalog Number
- 1700768-001 FDA UDI
- Primary DI / UDI-DI
- J00717007680011 FDA UDI
- FDA Product Code
- EBW FDA UDI
- GMDN Term
- Surgical power tool system control unit, line-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Surgical power tool system control unit, line-powered
Set Proimplant 3rd Gen Ca 20:1 L by Bien-Air Dental SA — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Surgical power tool system control unit, line-powered.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Bien-Air Dental SA
Sources (2)
- FDA UDI ff161e29-832e-4ccc-8d36-b43058f4472a 35 fields · synced Jun 10, 2026
- EUDAMED 1 fields · synced Jun 10, 2026