UDI device identifier
Dexcom G7 Receiver STK-AT-012
UDI device identifier 00386270002518 · Dexcom, Inc.
Key facts
| Primary DI | 00386270002518 |
|---|---|
| Brand name | Dexcom G7 Receiver |
| Version or model | STK-AT-012 |
| Company | Dexcom, Inc. |
| DUNS number | 123160736 |
| Product code | QBJ |
| GMDN term | Percutaneous interstitial fluid glucose monitoring system, electrochemical |
| Premarket submission | K213919 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 30, 2023 |
| Version date | Jul 14, 2025 |
| Description | G7 Receiver US |
At a glance
- 100–999 MAUDE reports citing this UDI
- Yes 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: