UDI device identifier
CVS Health Ovulation Test Kit
UDI device identifier 00050428082164 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Key facts
| Primary DI | 00050428082164 |
|---|---|
| Brand name | CVS Health |
| Version or model | Ovulation Test Kit |
| Company | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| DUNS number | 062312574 |
| Product code | CEP |
| GMDN term | Natural conception assistance kit |
| Premarket submission | K042280 |
| Device class | 1 | 2 |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 29, 2026 |
| Version date | Jul 7, 2026 |
| Description | A convenience kit consisting of 10 Ovulation Test devices and 1 One-Step 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: