Identity
- Trade Name
- PRIMODENT FDA UDI
- Generic Name
- Partial denture FDA UDI
- Device Name
- Resin Artificial Teeth FDA UDI
- Model / Reference
- PRV.S3SL3 FDA UDI
- Description
- Resin Artificial Teeth FDA UDI
Identifiers
- Catalog Number
- PRV.S3SL3 FDA UDI
- Primary DI / UDI-DI
- EPOLPRVS3SL3 FDA UDI
- FDA Product Code
- ELM FDA UDI
- GMDN Term
- Partial denture FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3590 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dry Heat Sterilization FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 3 Meter FDA UDI
Primodent by POLIDENT d.o.o. — 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
- POLIDENT d.o.o.
Sources (1)
- FDA UDI 132889af-f53a-40e0-8a28-bd6f8d119006 38 fields · synced May 31, 2026