UDI device identifier
KIMTECH PFE-XTRA LATEX EXAM GLOVES (S) 50501
UDI device identifier 00036000505016 · KIMBERLY-CLARK GLOBAL SALES, LLC
Key facts
| Primary DI | 00036000505016 |
|---|---|
| Brand name | KIMTECH PFE-XTRA LATEX EXAM GLOVES (S) |
| Version or model | 50501 |
| Catalog number | 50501-53 |
| Company | KIMBERLY-CLARK GLOBAL SALES, LLC |
| DUNS number | 830997032 |
| Product code | LYY |
| GMDN term | Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial |
| Premarket submission | K990539 |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 13, 2020 |
| Version date | Aug 18, 2025 |
| Description | Examination Gloves |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: