UDI device identifier
Answer™ Pregnancy Test 00022600408123
UDI device identifier 00022600408123 · CHURCH & DWIGHT CO., INC.
Key facts
| Primary DI | 00022600408123 |
|---|---|
| Brand name | Answer™ Pregnancy Test |
| Version or model | 00022600408123 |
| Company | CHURCH & DWIGHT CO., INC. |
| DUNS number | 001211952 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 19, 2019 |
| Version date | Sep 22, 2023 |
At a glance
- None MAUDE reports citing this UDI
- No 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: