UDI device identifier
RENASYS GO 66021814
UDI device identifier 00040565125572 · SMITH & NEPHEW MEDICAL LIMITED
Key facts
| Primary DI | 00040565125572 |
|---|---|
| Brand name | RENASYS GO |
| Version or model | 66021814 |
| Catalog number | 66021814 |
| Company | SMITH & NEPHEW MEDICAL LIMITED |
| DUNS number | 216344051 |
| Product code | OMP |
| GMDN term | Negative-pressure wound therapy system, battery-powered, reusable |
| Premarket submission | K152163 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Dec 1, 2016 |
| Version date | Sep 7, 2023 |
| Description | RENASYS GO QRG USA Only |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: