UDI device identifier
DURA-GUARD Dural Repair Patch DG0814SN
UDI device identifier 00085412531021 · SYNOVIS LIFE TECHNOLOGIES, INC.
Key facts
| Primary DI | 00085412531021 |
|---|---|
| Brand name | DURA-GUARD Dural Repair Patch |
| Version or model | DG0814SN |
| Catalog number | DG0814SN |
| Company | SYNOVIS LIFE TECHNOLOGIES, INC. |
| DUNS number | 017415781 |
| Product code | GXQ |
| GMDN term | Dura mater graft, bovine |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Oct 8, 2015 |
| Version date | Aug 10, 2023 |
| Description | DURA-GUARD Dural Repair Patch is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. DURA-GUARD Dural Repair Patch is chemically sterilized using ethanol and propylene oxide. DURA-GUARD Dural Repair… |
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: