UDI device identifier
LEADER 5412069
UDI device identifier 00096295133332 · Cardinal Health 110, Inc.
Key facts
| Primary DI | 00096295133332 |
|---|---|
| Brand name | LEADER |
| Version or model | 5412069 |
| Catalog number | 5412069 |
| Company | Cardinal Health 110, Inc. |
| DUNS number | 063997360 |
| Product code | LYY |
| GMDN term | Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial |
| Premarket submission | K093375 |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 23, 2018 |
| Version date | Jul 2, 2021 |
| Description | LDR GLOVE LATEX EXAM 100 SM PWF |
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: