UDI device identifier
CVS Liquid Bandage Spray 276670
UDI device identifier 00050428617656 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428617656 |
|---|---|
| Brand name | CVS Liquid Bandage Spray |
| Version or model | 276670 |
| Company | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| DUNS number | 062312574 |
| Product code | NEC |
| GMDN term | Skin-cover sealant |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 15, 2020 |
| Version date | Aug 7, 2020 |
| Description | Liquid Bandage in aerosol can |
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: