UDI device identifier
Becker® 25120
UDI device identifier 00763000333430 · MEDTRONIC PS MEDICAL, INC.
Key facts
| Primary DI | 00763000333430 |
|---|---|
| Brand name | Becker® |
| Version or model | 25120 |
| Company | MEDTRONIC PS MEDICAL, INC. |
| DUNS number | 089055867 |
| Product code | GWM |
| GMDN term | Cerebrospinal fluid external drainage kit |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 12, 2020 |
| Version date | Dec 23, 2024 |
| Description | EDMS II 25120 BECKER W/1-WAY VALVE |
At a glance
- 10–99 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: