UDI device identifier
LEADER 4902474
UDI device identifier 00096295124033 · Cardinal Health 110, Inc.
Key facts
| Primary DI | 00096295124033 |
|---|---|
| Brand name | LEADER |
| Version or model | 4902474 |
| Catalog number | 4902474 |
| Company | Cardinal Health 110, Inc. |
| DUNS number | 063997360 |
| Product code | KGX |
| GMDN term | Skin-cover adhesive strip, antimicrobial |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 18, 2019 |
| Version date | Mar 8, 2023 |
| Description | Advanced Antibacterial Clear Waterproof Strong Strips; XL Adhesive Bandages; Triple Pad Technology; Helps Prevent Infection; 3x Absorbent Pad; Pain Free Film; Extra Large; 2 IN. x 4 IN.; Antibacterial Agent Benzalkonium Chloride 0.1% |
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: