FDA device listing
Coronary Drug-Eluting Stent
FDA device listing 1943502110 · Sotera Health LLC
Key facts
| Owner/operator | Sotera Health LLC |
|---|---|
| Owner/operator number | 10029425 |
| Product codes | NIQ |
| Device names | NIQ - Coronary Drug-Eluting Stent |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.NIQ |
| Review panels | Cardiovascular |
| Registered establishments | Sterigenics UK Limited, Sterigenics US LLC |
| Establishment registrations | 2011171, 3008132398 |
| FEI numbers | 2011171, 3002807091 |
| 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