UDI device identifier
Universal Screw Removal Kit Universal Screw Removal Kit
UDI device identifier 00083208003332 · Suncoast Dental, Inc
Key facts
| Primary DI | 00083208003332 |
|---|---|
| Brand name | Universal Screw Removal Kit |
| Version or model | Universal Screw Removal Kit |
| Catalog number | Universal Screw Removal Kit |
| Company | Suncoast Dental, Inc |
| DUNS number | 078352849 |
| Product code | DZA |
| GMDN term | Fixture/appliance dental drill bit, single-use |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 29, 2025 |
| Version date | Oct 7, 2025 |
| Description | Universal Screw Removal Kit - 20 Piece Instrument Kit in Autoclavable Case |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: