UDI device identifier
TRUEplus TRUEplus 5 bevel Pen Needle 32G/4mm - 100ct box
UDI device identifier 00021292010805 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292010805 |
|---|---|
| Brand name | TRUEplus |
| Version or model | TRUEplus 5 bevel Pen Needle 32G/4mm - 100ct box |
| Catalog number | S6H01A32-100 |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | FMI |
| GMDN term | Autoinjector needle |
| Premarket submission | K171144 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 12, 2018 |
| Version date | Jul 6, 2018 |
| Description | TRUEplus 5 bevel Pen Needle 32G/4mm - 100ct box |
At a glance
- 1–9 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: