UDI device identifier
TRUEplus TRUEplus Safety Lancets
UDI device identifier 00021292010522 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292010522 |
|---|---|
| Brand name | TRUEplus |
| Version or model | TRUEplus Safety Lancets |
| Catalog number | S7H01RN28-25 |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | FMK |
| GMDN term | Manual blood lancing device, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 23, 2020 |
| Version date | Dec 23, 2022 |
| Description | TRUEplus Safety Lancets |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: