FDA device listing
V-707377 USS Module
FDA device listing 1850478006 · Jaeger Medical GmbH
Key facts
| Proprietary names | V-707377 USS Module |
|---|---|
| Owner/operator | Jaeger Medical GmbH |
| Owner/operator number | 10092652 |
| Product codes | BXP |
| Device names | BXP - Transducer, Gas Flow |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.2885 |
| Review panels | Anesthesiology |
| Registered establishments | Jaeger Medical America Inc., Jaeger Medical GmbH |
| Establishment registrations | 9615102, 3033959233 |
| FEI numbers | 1000271197, 3033959233 |
| Establishment operations | Complaint File Establishment, Repackager/Relabeler, 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