Identity
- Trade Name
- Vivid PMMA Standard System FDA UDI
- Generic Name
- Dental appliance fabrication material, ceramic FDA UDI
- Device Name
- 98x25 A2 FDA UDI
- Model / Reference
- Q250170 FDA UDI
- Description
- 98x25 A2 FDA UDI
Identifiers
- Primary DI / UDI-DI
- D724Q2501701 FDA UDI
- FDA Product Code
- ELL FDA UDI
- GMDN Term
- Dental appliance fabrication material, ceramic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3920 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental appliance fabrication material, ceramic
The Vivid PMMA Standard System is a high-performance dental appliance fabrication material, designed for creating implantable and removable restorations using manual or computer-aided design/computer-aided manufacturing (CAD/CAM) technology.
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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
- Pearson Dental Supplies, Inc.
Sources (1)
- FDA UDI 5aeb5966-740d-44f0-9802-8cd4d709f082 33 fields · synced Jul 5, 2026