FDA device listing
Aspi Hydrophobic Filter Set - ASP-HFS,AspiPump 90D - ASPI-90D,AspiPump Foot Switch - ASP - FS,Aspi Suction Bottle with…
FDA device listing 1014143503 · Allwin Medical Devices
Key facts
| Proprietary names | Aspi Hydrophobic Filter Set - ASP-HFS,AspiPump 90D - ASPI-90D,AspiPump Foot Switch - ASP - FS,Aspi Suction Bottle with Connector - ASP-SB,Aspi Suction Line with Luer Lock Connectors - ASP - SL |
|---|---|
| Owner/operator | Allwin Medical Devices |
| Owner/operator number | 9036357 |
| Product codes | GCX |
| Device names | GCX - Apparatus, Suction, Operating-Room, Wall Vacuum Powered |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.6740 |
| Review panels | General Hospital |
| Registered establishments | Allwin Medical Devices Pvt. Ltd. |
| Establishment registrations | 9617744 |
| FEI numbers | 3006279007 |
| 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