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Tuff-Temp™ Plus Provisional Veneer, Crown & Bridge Resin
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- TUFF-TEMP™ PLUS PROVISIONAL VENEER, CROWN & BRIDGE RESIN FDA UDI
- Generic Name
- Dental composite resin FDA UDI
- Device Name
- 5 mL AUTOMIX SYRINGE, 8 AUTOMIX TIPS, 3mL Glaze FDA UDI
- Model / Reference
- TTP5 FDA UDI
- Description
- 5 mL AUTOMIX SYRINGE, 8 AUTOMIX TIPS, 3mL Glaze FDA UDI
Identifiers
- Primary DI / UDI-DI
- D701TTP52 FDA UDI
- FDA Product Code
- EBG FDA UDI
- GMDN Term
- Dental composite resin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3770 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental composite resin
Tuff-Temp™ Plus Provisional Veneer, Crown & Bridge Resin by Pulpdent Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Pulpdent Corporation
Sources (1)
- FDA UDI 0739e521-55e7-4ac2-9d3f-7fa263824f5f 33 fields · synced Jun 9, 2026