UDI device identifier
Tandem Diabetes 3mL LL WITH CO-PACKED NEEDLE 26Gx3/8’’ 1001215
UDI device identifier 00020221012156 · Exel International
Key facts
| Primary DI | 00020221012156 |
|---|---|
| Brand name | Tandem Diabetes 3mL LL WITH CO-PACKED NEEDLE 26Gx3/8’’ |
| Version or model | 1001215 |
| Catalog number | 1001215 |
| Company | Exel International |
| DUNS number | 180572216 |
| Product code | FMF |
| GMDN term | General-purpose syringe/needle |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 17, 2023 |
| Version date | Jun 8, 2026 |
| Description | Tandem Diabetes 3mL LL WITH CO-PACKED NEEDLE 26Gx3/8’’ 100/BX, 1000/CS |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- Yes 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: