UDI device identifier
First Response Early Result Pregnancy Test 00022600020141
UDI device identifier 00022600020141 · CHURCH & DWIGHT CO., INC.
Key facts
| Primary DI | 00022600020141 |
|---|---|
| Brand name | First Response Early Result Pregnancy Test |
| Version or model | 00022600020141 |
| Company | CHURCH & DWIGHT CO., INC. |
| DUNS number | 001211952 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Premarket submission | K123436 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 25, 2019 |
| Version date | Jul 6, 2023 |
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: