UDI device identifier
Vermed LWG-2090029GR
UDI device identifier 00009336002603 · GRAPHIC CONTROLS ACQUISITION CORP
Key facts
| Primary DI | 00009336002603 |
|---|---|
| Brand name | Vermed |
| Version or model | LWG-2090029GR |
| Catalog number | LWG-2090029GR |
| Company | GRAPHIC CONTROLS ACQUISITION CORP |
| DUNS number | 002111896 |
| Product code | DSA |
| GMDN term | Electrocardiographic lead set, reusable |
| Premarket submission | K992524 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Jun 6, 2024 |
| Description | Leadwire Safety Din To Snap, 29" Green-RL |
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: