UDI device identifier
InTENSity DQ8000
UDI device identifier 00092237615218 · Drive Devilbiss Healthcare
Key facts
| Primary DI | 00092237615218 |
|---|---|
| Brand name | InTENSity |
| Version or model | DQ8000 |
| Company | Drive Devilbiss Healthcare |
| DUNS number | 867673159 |
| Product code | GZJ |
| GMDN term | Physical therapy transcutaneous neuromuscular electrical stimulation system |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 12, 2016 |
| Version date | Jun 22, 2026 |
| Description | InTENSity CX4 Professional |
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: