UDI device identifier
GUIDOR 5000
UDI device identifier 00070942000031 · SUNSTAR AMERICAS, INC.
Key facts
| Primary DI | 00070942000031 |
|---|---|
| Brand name | GUIDOR |
| Version or model | 5000 |
| Catalog number | MC |
| Company | SUNSTAR AMERICAS, INC. |
| DUNS number | 025066358 |
| Product code | NPK |
| GMDN term | Pliable-polymer dental regeneration membrane, bioabsorbable, ligated |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Oct 13, 2015 |
| Version date | Jun 16, 2023 |
| Description | GUIDOR® Bioresorbable Matrix Barrier |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: