UDI device identifier
CVS Health Wide-Tip Triple Test Pregnancy Test Kit
UDI device identifier 00050428079263 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428079263 |
|---|---|
| Brand name | CVS Health |
| Version or model | Wide-Tip Triple Test Pregnancy Test Kit |
| Company | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| DUNS number | 062312574 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Premarket submission | K042280 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 28, 2024 |
| Version date | Aug 21, 2026 |
| Description | A convenience kit consisting of 1 Advanced Early Result Test, 1 Digital Wide-Tip Test and 1 Advanced One Step Test |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: