UDI device identifier
Omnipod 5 Pod POD-OMNI-I1-6720
UDI device identifier 10385083000527 · Insulet Corporation
Key facts
| Primary DI | 10385083000527 |
|---|---|
| Brand name | Omnipod 5 Pod |
| Version or model | POD-OMNI-I1-6720 |
| Company | Insulet Corporation |
| DUNS number | 051334402 |
| Product code | QFG |
| GMDN term | Ambulatory insulin infusion pump/interstitial glucose monitoring system |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Feb 22, 2024 |
| Version date | Dec 4, 2025 |
| Description | Omnipod 5 Pod |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: