UDI device identifier
KIMTECH VISTA NITRILE EXAM (XL) 62829
UDI device identifier 00036000628296 · KIMBERLY-CLARK GLOBAL SALES, LLC
Key facts
| Primary DI | 00036000628296 |
|---|---|
| Brand name | KIMTECH VISTA NITRILE EXAM (XL) |
| Version or model | 62829 |
| Catalog number | 62829-00 |
| Company | KIMBERLY-CLARK GLOBAL SALES, LLC |
| DUNS number | 830997032 |
| 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 15, 2021 |
| Version date | Apr 23, 2021 |
| Description | Examination Gloves |
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: