Identity
- Trade Name
- C-PLAST FDA UDI
- Generic Name
- Dental base plate FDA UDI
- Device Name
- C-Plast Polymer 500g F34 FDA UDI
- Model / Reference
- 672722 FDA UDI
- Description
- C-Plast Polymer 500g F34 FDA UDI
Identifiers
- Catalog Number
- 672722 FDA UDI
- Primary DI / UDI-DI
- 07630813440033 FDA UDI
- FDA Product Code
- EBH FDA UDI
- GMDN Term
- Dental base plate FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3670 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: Dental base plate
C-Plast by Candulor AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental base plate.
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- LIGHT RESIN PLATE — YAMAHACHI DENTAL MFG., CO. · Class I
- Wrights — Wright Health Group , Ltd. · Class I
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
- Candulor AG
Sources (1)
- FDA UDI 72368889-7a8c-4e42-ae34-e3b925610bff 34 fields · synced May 30, 2026