UDI device identifier
VeriQuick 4969672605
UDI device identifier 00049696726054 · FOURSTAR GROUP INC.
Key facts
| Primary DI | 00049696726054 |
|---|---|
| Brand name | VeriQuick |
| Version or model | 4969672605 |
| Company | FOURSTAR GROUP INC. |
| DUNS number | 656091279 |
| Product code | NGE |
| GMDN term | Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 27, 2017 |
| Version date | Jun 10, 2022 |
| Description | VeriQuick Ovulation Predictor Test for Family Dollar |
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: