UDI device identifier
PSD gel PSDGEL3PKWTIPS
UDI device identifier 00085412531434 · SYNOVIS LIFE TECHNOLOGIES, INC.
Key facts
| Primary DI | 00085412531434 |
|---|---|
| Brand name | PSD gel |
| Version or model | PSDGEL3PKWTIPS |
| Catalog number | PSDGel3pkwTips |
| Company | SYNOVIS LIFE TECHNOLOGIES, INC. |
| DUNS number | 017415781 |
| Product code | FTM |
| GMDN term | Staple line-reinforcement strip gel |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Oct 5, 2015 |
| Version date | Oct 30, 2023 |
| Description | PSD Gel is prepared from Hydroxypropyl Methyl Cellulose, Propylene Glycol, and water. The PSD Gel is used to bond the Peri-Strips Dry pericardium strips onto the surgical stapler forks until the stapler is positioned and fired. |
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: