Identity
- Trade Name
- FotoDent® tray FDA UDI
- Generic Name
- Dental impression tray material FDA UDI
- Device Name
- No. FDA UDI
- Model / Reference
- D35300 FDA UDI
- Description
- No. FDA UDI
Identifiers
- Catalog Number
- D35300 FDA UDI
- Primary DI / UDI-DI
- E239D353001 FDA UDI
- FDA Product Code
- EBH FDA UDI
- GMDN Term
- Dental impression tray material FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3670 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
FotoDent® tray by Dreve Dentamid GmbH — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dreve Dentamid GmbH
Sources (1)
- FDA UDI a4e93284-8d72-4787-bc00-541662a2e68e 37 fields · synced Jun 1, 2026