UDI device identifier
TRUEplus TRUEplus SINGLE-USE INSULIN syringes 31 gauge needle 1.0cc insulin
UDI device identifier 00021292005887 · TRIVIDIA HEALTH, INC.
Key facts
| Primary DI | 00021292005887 |
|---|---|
| Brand name | TRUEplus |
| Version or model | TRUEplus SINGLE-USE INSULIN syringes 31 gauge needle 1.0cc insulin |
| Company | TRIVIDIA HEALTH, INC. |
| DUNS number | 151810868 |
| Product code | FMF |
| GMDN term | Insulin syringe/needle, basic |
| Premarket submission | K993017 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 20, 2016 |
| Version date | Aug 30, 2024 |
| Description | TRUEplus SINGLE-USE INSULIN syringes 31 gauge needle 1.0cc insulin |
At a glance
- 10–99 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: