UDI device identifier
TRUEplus TRUEplus Ketone Test Strips
UDI device identifier 00021292008178 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292008178 |
|---|---|
| Brand name | TRUEplus |
| Version or model | TRUEplus Ketone Test Strips |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | JIN |
| GMDN term | Urine ketone IVD, kit, rapid colorimetric, clinical |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 21, 2020 |
| Version date | Aug 19, 2025 |
| Description | TRUEplus Ketone Test Strips |
At a glance
- 10–99 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: