UDI device identifier
CVS Health Triple Test Pregnancy Test Kit
UDI device identifier 00050428417027 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428417027 |
|---|---|
| Brand name | CVS Health |
| Version or model | 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 27, 2023 |
| Version date | Dec 24, 2024 |
| Description | A convenience kit consisting of 1 One Step Pregnancy Test, 1 Early Result Pregnancy Test and 1 Digital Yes+ No- Pregnancy 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: