UDI device identifier
TRUEplus Sunmark TRUEplus Sterile Lancets
UDI device identifier 00010939701442 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00010939701442 |
|---|---|
| Brand name | TRUEplus |
| Version or model | Sunmark TRUEplus Sterile Lancets |
| Catalog number | S1054DB30-100 |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | QRK |
| GMDN term | Blood lancing device tip |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 27, 2020 |
| Version date | Aug 30, 2024 |
| Description | Sunmark TRUEplus Sterile Lancets |
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: