UDI device identifier
CVS CVS739091V2
UDI device identifier 00050428167274 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428167274 |
|---|---|
| Brand name | CVS |
| Version or model | CVS739091V2 |
| Catalog number | CVS739091V2 |
| Company | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| DUNS number | 062312574 |
| Product code | FMK |
| GMDN term | Manual blood lancing device, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 9, 2026 |
| Version date | Apr 17, 2026 |
| Description | Lancing Device, For Capillary Blood Sampling, 30G |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: