UDI device identifier
VeriQuick 11012450MA
UDI device identifier 00049696737739 · FOURSTAR GROUP INC.
Key facts
| Primary DI | 00049696737739 |
|---|---|
| Brand name | VeriQuick |
| Version or model | 11012450MA |
| Company | FOURSTAR GROUP INC. |
| DUNS number | 656091279 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, enzyme immunoassay (EIA) |
| Premarket submission | K150022 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 26, 2021 |
| Version date | Oct 14, 2024 |
| Description | PREGNANCY TEST 1CT |
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: