FDA device listing
HemaCarotid Patch,Hemagard Carotid patch,Hemagard Knitted,HemaPatch Vascular Patches,InterGard and Intergard RS Vascular…
FDA device listing 1614161673 · Sotera Health LLC
Key facts
| Proprietary names | HemaCarotid Patch,Hemagard Carotid patch,Hemagard Knitted,HemaPatch Vascular Patches,InterGard and Intergard RS Vascular Prostheses |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | DSY |
| Device names | DSY - Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.3450 |
| Review panels | Cardiovascular |
| Registered establishments | Sterigenics Italy SpA |
| Establishment registrations | 3010407203 |
| FEI numbers | 3010407203 |
| Establishment operations | Contract Sterilizer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database