UDI device identifier
TRUE FOCUS TRUE FOCUS Self Monitoring Test Strip - 50ct
UDI device identifier 00021292008956 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292008956 |
|---|---|
| Brand name | TRUE FOCUS |
| Version or model | TRUE FOCUS Self Monitoring Test Strip - 50ct |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | LFR |
| GMDN term | Glucose monitoring system IVD, home-use |
| Premarket submission | K131013 |
| Device class | 1 | 2 |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 21, 2017 |
| Version date | Jul 6, 2018 |
| Description | TRUE FOCUS Self Monitoring Test Strip - 50ct |
At a glance
- 10–99 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: