UDI device identifier
VeriQuick 64410323
UDI device identifier 00049696676038 · FOURSTAR GROUP INC.
Key facts
| Primary DI | 00049696676038 |
|---|---|
| Brand name | VeriQuick |
| Version or model | 64410323 |
| Company | FOURSTAR GROUP INC. |
| DUNS number | 656091279 |
| Product code | NGA |
| GMDN term | Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 11, 2026 |
| Version date | Jun 19, 2026 |
| Description | VQ MENOPAUSE TEST KIT |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: