UDI device identifier
Vermed PR-A520-1013P
UDI device identifier 00009336006298 · GRAPHIC CONTROLS ACQUISITION CORP
Key facts
| Primary DI | 00009336006298 |
|---|---|
| Brand name | Vermed |
| Version or model | PR-A520-1013P |
| Catalog number | PR-A520-1013P |
| Company | GRAPHIC CONTROLS ACQUISITION CORP |
| DUNS number | 002111896 |
| Product code | DQA |
| GMDN term | Telemetric pulse oximeter |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Mar 29, 2018 |
| Description | N Kohden comp.(new)Adult Reusable SpO2 Finger Sensor,5'/1.6m |
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: