FDA device listing
Salter Labs In Line Water Trap
FDA device listing 1540799392 · SunMed "also trading as AirLife"
Key facts
| Proprietary names | Salter Labs In Line Water Trap |
|---|---|
| Owner/operator | SunMed "also trading as AirLife" |
| Owner/operator number | 9038422 |
| Product codes | BYH |
| Device names | BYH - Drain, Tee (Water Trap) |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5995 |
| Review panels | Anesthesiology |
| Registered establishments | Salter Labs, Salter Labs de Mexico de S.A. de C.V. |
| Establishment registrations | 3004748541, 3010272829 |
| FEI numbers | 3004748541, 3010272829 |
| Establishment operations | Manufacturer, Specification Developer |
| 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