UDI device identifier
Intellinetix 07230
UDI device identifier 00082161072300 · BROWNMED, INC.
Key facts
| Primary DI | 00082161072300 |
|---|---|
| Brand name | Intellinetix |
| Version or model | 07230 |
| Company | BROWNMED, INC. |
| DUNS number | 091999771 |
| Product code | ISA |
| GMDN term | Circulatory/musculoskeletal vibration therapy unit, hand-held |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 12, 2020 |
| Version date | Aug 20, 2020 |
| Description | Vibrating therapeutic massager |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: