UDI device identifier
VIRTU-CLEAN GL-NCREX
UDI device identifier 00075289715570 · TRANZONIC COMPANIES, THE
Key facts
| Primary DI | 00075289715570 |
|---|---|
| Brand name | VIRTU-CLEAN |
| Version or model | GL-NCREX |
| Catalog number | GL-NCREX |
| Company | TRANZONIC COMPANIES, THE |
| DUNS number | 007900020 |
| Product code | LZA |
| GMDN term | Nitrile examination/treatment glove, non-powdered, non-antimicrobial |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 25, 2024 |
| Version date | Dec 3, 2024 |
| Description | VIRTU-CLEAN NITRILE CLEAN ROOM, PF, EXAM GLOVES, XL, 10/100 |
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: