Identity
- Trade Name
- Regofix opak FDA UDI
- Generic Name
- Silicone dental impression material FDA UDI
- Device Name
- Our classical bite registration material, fast, hard and precise. Very good cutting and milling characteristics. 8 x 50 ml double cartridges. FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Our classical bite registration material, fast, hard and precise. Very good cutting and milling characteristics. 8 x 50 ml double cartridges. FDA UDI
Identifiers
- Catalog Number
- D504875 FDA UDI
- Primary DI / UDI-DI
- E239D5048751 FDA UDI
- FDA Product Code
- ELW FDA UDI
- GMDN Term
- Silicone dental impression material FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3660 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
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Regofix opak by Dreve Dentamid GmbH — 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
- Dreve Dentamid GmbH
Sources (1)
- FDA UDI 9df80f56-6678-4b77-b1d7-3c24bb0b708e 36 fields · synced May 30, 2026