FDA device listing
AMSCO Drying Cabinets (QB-RR),Connectors for Reliance 6000 Series Endoscope Storage Cabinet (QB-RR),Drying Cabinet…
FDA device listing 1459484980 · STERIS Corporation
Key facts
| Proprietary names | AMSCO Drying Cabinets (QB-RR),Connectors for Reliance 6000 Series Endoscope Storage Cabinet (QB-RR),Drying Cabinet Connectors (QB-RR),Reliance 5000 Series Endoscope Storage Cabinet (QB-RR),Reliance 6000 Series Endoscope Storage Cabinet (QB-RR),Reliance 6500 Series Endoscope Drying and Storage Cabinet (MM-MF, PY-SD),Tubing Sets for Reliance 6500 Series Endoscope Drying and Storage Cabinet (HP-MF… |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10078069 |
| Product codes | PUP |
| Device names | PUP - Endoscope Maintenance System |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | STERIS Canada ULC, STERIS Corporation |
| Establishment registrations | 9680353, 3000251274, 3003950207 |
| FEI numbers | 3000251274, 3003950207, 3004097451 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| 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