UDI device identifier
ENTity XL Nasopharyngoscope F014721
UDI device identifier 00085119004132 · OPTIM LLC
Key facts
| Primary DI | 00085119004132 |
|---|---|
| Brand name | ENTity XL Nasopharyngoscope |
| Version or model | F014721 |
| Company | OPTIM LLC |
| DUNS number | 052927001 |
| Product code | EOB |
| GMDN term | Flexible fibreoptic nasopharyngoscope |
| Premarket submission | K080622 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 19, 2016 |
| Version date | Apr 24, 2020 |
| Description | ENTity XL NasoView Flexible LED Nasopharyngoscope |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: