FDA device listing
22/10mm Tube
FDA device listing 1928032829 · CHEEN HOUNG ENT. CO. LTD.
Key facts
| Proprietary names | 22/10mm Tube |
|---|---|
| Owner/operator | CHEEN HOUNG ENT. CO. LTD. |
| Owner/operator number | 8043061 |
| 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 | CHEEN HOUNG ENT. CO. LTD. |
| Establishment registrations | 9612374 |
| FEI numbers | 3002806674 |
| Establishment operations | Foreign Exporter |
| 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