UDI device identifier
Preempt Plus RTU (US) 32oz
UDI device identifier 00068460506104 · Virox Technologies Inc
Key facts
| Primary DI | 00068460506104 |
|---|---|
| Brand name | Preempt Plus RTU (US) |
| Version or model | 32oz |
| Company | Virox Technologies Inc |
| DUNS number | 255343022 |
| Product code | LRJ |
| GMDN term | Medical device disinfection agent |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 8, 2021 |
| Version date | Apr 4, 2023 |
At a glance
- None 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: