UDI device identifier
First Response™ Ovulation Daily Digital Ovulation Test 00022600408000
UDI device identifier 00022600408000 · CHURCH & DWIGHT CO., INC.
Key facts
| Primary DI | 00022600408000 |
|---|---|
| Brand name | First Response™ Ovulation Daily Digital Ovulation Test |
| Version or model | 00022600408000 |
| Company | CHURCH & DWIGHT CO., INC. |
| DUNS number | 001211952 |
| Product code | CEP |
| GMDN term | Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical |
| Premarket submission | K973310 |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 14, 2016 |
| Version date | Jun 10, 2022 |
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: