UDI device identifier
Peri-Strips Dry with Veritas Collagen Matrix PSD6006ETSV
UDI device identifier 00085412531748 · SYNOVIS LIFE TECHNOLOGIES, INC.
Key facts
| Primary DI | 00085412531748 |
|---|---|
| Brand name | Peri-Strips Dry with Veritas Collagen Matrix |
| Version or model | PSD6006ETSV |
| Catalog number | PSD6006ETSV |
| Company | SYNOVIS LIFE TECHNOLOGIES, INC. |
| DUNS number | 017415781 |
| Product code | FTM |
| GMDN term | Staple line-reinforcement strip |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Oct 5, 2015 |
| Version date | Oct 30, 2023 |
| Description | Peri-Strips Dry with Veritas Collagen Matrix (PSD-V) is prepared from dehydrated bovine pericardium procured from cattle under 30 months of age in the United States. One (1) tube of PSD Gel (Gel) is provided for every two (2) pouches of PSD-V. The Gel is used to create a temporary bond between the… |
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: