FDA device listing
Tubing, Pressure And Accessories
FDA device listing 1098933778 · RESMED CORP.
Key facts
| Owner/operator | RESMED CORP. |
|---|---|
| Owner/operator number | 9002319 |
| Product codes | BYX |
| Device names | BYX - Tubing, Pressure And Accessories |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5860 |
| Review panels | Anesthesiology |
| Registered establishments | ResMed Asia Pte. Ltd., ResMed Corp, RESMED CORP, RESMED PTY LTD., ResMed West Coast Warehouse, RMO |
| Establishment registrations | 3004604967, 3007009701, 3007573469, 3011205710, 3017684630, 3030970580 |
| FEI numbers | 1000115734, 3004604967, 3007009701, 3011205710, 3017684630, 3030970580 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, Manufacturer |
| 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