UDI device identifier
CABVI/High Five 72-10500R
UDI device identifier 00071503216816 · Ansell Healthcare Product
Key facts
| Primary DI | 00071503216816 |
|---|---|
| Brand name | CABVI/High Five |
| Version or model | 72-10500R |
| Catalog number | 72-10500R |
| Company | Ansell Healthcare Product |
| DUNS number | 111267330 |
| 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 | Apr 14, 2022 |
| Version date | Apr 22, 2022 |
| Description | CABVI PF Cobalt Nitrile 72-1050xR SIZE XS, Nitrile Powder-Free Examination Glove |
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: