UDI device identifier
TRUEplus TRUEplus Pen Needles 5Bevel - 32G 4mm - 50ct box
UDI device identifier 00021292014995 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292014995 |
|---|---|
| Brand name | TRUEplus |
| Version or model | TRUEplus Pen Needles 5Bevel - 32G 4mm - 50ct box |
| Catalog number | S6H01A32-50 |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | FMI |
| GMDN term | Autoinjector needle |
| Premarket submission | K180720 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Aug 22, 2023 |
| Version date | Aug 30, 2023 |
| Description | TRUEplus Pen Needles 5Bevel - 32G 4mm - 50ct box |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: