UDI device identifier
LEADER 5297460
UDI device identifier 00096295130362 · Cardinal Health 110, Inc.
Key facts
| Primary DI | 00096295130362 |
|---|---|
| Brand name | LEADER |
| Version or model | 5297460 |
| Catalog number | 5297460 |
| Company | Cardinal Health 110, Inc. |
| DUNS number | 063997360 |
| Product code | NUH |
| GMDN term | Analgesic transcutaneous electrical nerve stimulation system |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 14, 2017 |
| Version date | Oct 12, 2022 |
| Description | LDR Electro TENS replacement gel pads 3 ea |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: