UDI device identifier
TRUEdraw TRUEdraw Lancing Device
UDI device identifier 00021292142018 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292142018 |
|---|---|
| Brand name | TRUEdraw |
| Version or model | TRUEdraw Lancing Device |
| Catalog number | M2H01-81 |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | QRL |
| GMDN term | Manual blood lancing device, reusable |
| Premarket submission | K221072 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Dec 14, 2020 |
| Version date | Nov 17, 2022 |
| Description | TRUEdraw Lancing Device |
At a glance
- None 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: