UDI device identifier
GUM® 800
UDI device identifier 00070942751469 · SUNSTAR AMERICAS, INC.
Key facts
| Primary DI | 00070942751469 |
|---|---|
| Brand name | GUM® |
| Version or model | 800 |
| Catalog number | CQA |
| Company | SUNSTAR AMERICAS, INC. |
| DUNS number | 025066358 |
| Product code | QJC |
| GMDN term | Dental caries detecting stain |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 29, 2021 |
| Version date | Sep 16, 2024 |
| Description | RED-COTE® Plaque Disclosing Tablets |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: