UDI device identifier
Dexcom Clarity 350-0011
UDI device identifier 00038270000451 · Dexcom, Inc.
Key facts
| Primary DI | 00038270000451 |
|---|---|
| Brand name | Dexcom Clarity |
| Version or model | 350-0011 |
| Company | Dexcom, Inc. |
| DUNS number | 123160736 |
| Product code | PHV |
| GMDN term | Percutaneous interstitial fluid glucose monitoring system, electrochemical |
| Premarket submission | DEN140016 |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Dec 20, 2016 |
| Version date | Jul 14, 2025 |
| Description | Data Manager Software |
At a glance
- None 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: