UDI device identifier
Bravo FGS-0636
UDI device identifier 07290101369714 · Given Imaging, Inc.
Key facts
| Primary DI | 07290101369714 |
|---|---|
| Brand name | Bravo |
| Version or model | FGS-0636 |
| Company | Given Imaging, Inc. |
| DUNS number | 090073722 |
| Product code | FFT |
| GMDN term | Gastrointestinal telemetric monitoring system |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 20, 2018 |
| Version date | Nov 15, 2024 |
| Description | Bravo™ CF capsule delivery dev,1-pk |
At a glance
- 100–999 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: