UDI device identifier
FreeStyle Libre 3 72080
UDI device identifier 00357599819002 · ABBOTT DIABETES CARE INC
Key facts
| Primary DI | 00357599819002 |
|---|---|
| Brand name | FreeStyle Libre 3 |
| Version or model | 72080 |
| Catalog number | 72080 |
| Company | ABBOTT DIABETES CARE INC |
| DUNS number | 966390890 |
| Product code | QLG |
| GMDN term | Percutaneous interstitial fluid glucose monitoring system, electrochemical |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Jun 23, 2022 |
| Version date | Jul 14, 2025 |
| Description | FreeStyle Libre 3 Sensor Kit NFRS |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: