Identity
- Trade Name
- Zitemp FDA UDI
- Generic Name
- Zinc oxide eugenol dental cement FDA UDI
- Model / Reference
- 15g powder FDA UDI
Identifiers
- Catalog Number
- 30016 FDA UDI
- Primary DI / UDI-DI
- D9673001600 FDA UDI
- FDA Product Code
- EMB FDA UDI
- GMDN Term
- Zinc oxide eugenol dental cement FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3275 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
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
Yes
FDA UDI
Category: Zinc oxide eugenol dental cement
Zitemp by Prevest Denpro Limited — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Prevest Denpro Limited
Sources (1)
- FDA UDI 8da42ccc-b21a-450a-94fa-cc1f4a88ecfe 33 fields · synced Jun 7, 2026