UDI device identifier
CVS Health 638389
UDI device identifier 00050428029572 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428029572 |
|---|---|
| Brand name | CVS Health |
| Version or model | 638389 |
| Company | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| DUNS number | 062312574 |
| Product code | NGL |
| GMDN term | Multiple drugs of abuse IVD, kit, rapid ICT, clinical |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 10, 2025 |
| Version date | Jun 18, 2025 |
| Description | CVS HEALTH Home Drug Test- Fentanyl Rapid Dip |
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: