UDI device identifier
GoodSense 180410000231
UDI device identifier 00180410000231 · GEISS, DESTIN & DUNN, INC
Key facts
| Primary DI | 00180410000231 |
|---|---|
| Brand name | GoodSense |
| Version or model | 180410000231 |
| Company | GEISS, DESTIN & DUNN, INC |
| DUNS number | 076059836 |
| Product code | FQM |
| GMDN term | Pressure bandage, non-latex, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 28, 2020 |
| Version date | Dec 8, 2021 |
| Description | Tender Tape, 2 IN x 5 YDS (50 mm x 4.5 m) stretched; 2 IN x 2.2 YDS (50 mm x 2 m) |
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: