UDI device identifier
Trilogy Evo Trilogy Evo, USA
UDI device identifier 00606959051942 · Respironics, Inc.
Key facts
| Primary DI | 00606959051942 |
|---|---|
| Brand name | Trilogy Evo |
| Version or model | Trilogy Evo, USA |
| Catalog number | DS2110X11B |
| Company | Respironics, Inc. |
| DUNS number | 080728314 |
| Product code | CBK |
| GMDN term | Portable electric ventilator |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | May 13, 2022 |
| Version date | Feb 6, 2023 |
| Description | Trilogy Evo, USA |
At a glance
- 1,000+ 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: