UDI device identifier
CVS 557102
UDI device identifier 00050428396841 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428396841 |
|---|---|
| Brand name | CVS |
| Version or model | 557102 |
| Company | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| DUNS number | 062312574 |
| Product code | LFD |
| GMDN term | Artificial saliva |
| Device class | Unclassified |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 23, 2022 |
| Version date | Feb 18, 2025 |
| Description | Dry Mouth Mouthwash Mint Flavor 16 FL OZ (473 mL) LGG43 |
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: