UDI device identifier
ProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision 800022-14
UDI device identifier 00180668000403 · UROMEDICA INC
Key facts
| Primary DI | 00180668000403 |
|---|---|
| Brand name | ProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision |
| Version or model | 800022-14 |
| Company | UROMEDICA INC |
| DUNS number | 080378479 |
| GMDN term | Hydraulic male urinary incontinence treatment system |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Jul 15, 2016 |
| Version date | Jan 23, 2019 |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
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: