FDA device listing
MEGASAN Central System Medical Pressure Regulators, MEGASAN Cylinder Type Medical Pressure Regulators, MEGASAN Central S
FDA device listing 1077257656 · Megasan Medikal Gaz Sistemleri Tibbi Alet ve Cihazlar San. T
Key facts
| Proprietary names | MEGASAN Central System Medical Pressure Regulators, MEGASAN Cylinder Type Medical Pressure Regulators, MEGASAN Central S |
|---|---|
| Owner/operator | Megasan Medikal Gaz Sistemleri Tibbi Alet ve Cihazlar San. T |
| Owner/operator number | 10089436 |
| Product codes | BXH |
| Device names | BXH - Gauge, Gas Pressure, Cylinder/Pipeline |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.2610 |
| Review panels | Anesthesiology |
| Registered establishments | MEGASAN MEDIKAL GAZ SISTEMLERI TIBBI ALET VE CIHAZLAR SAN. TIC. A. S. |
| Establishment registrations | 3030128613 |
| FEI numbers | 3030128613 |
| Establishment operations | 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