UDI device identifier
BREEZE 31216201
UDI device identifier 00090891949373 · DOLGENCORP, LLC
Key facts
| Primary DI | 00090891949373 |
|---|---|
| Brand name | BREEZE |
| Version or model | 31216201 |
| Company | DOLGENCORP, LLC |
| DUNS number | 068331990 |
| Product code | NRC |
| GMDN term | Menstrual pad, scented |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 17, 2023 |
| Version date | Jan 25, 2023 |
| Description | ULTRA THIN FOAM PAD WING LONG SUPER SCENTED 26 CT |
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: