FDA device listing
Humidifier, Respiratory Gas, (Direct Patient Interface)
FDA device listing 1700229940 · Vincent Medical(Dongguan)Technology Company Limited
Key facts
| Owner/operator | Vincent Medical(Dongguan)Technology Company Limited |
|---|---|
| Owner/operator number | 10076353 |
| Premarket submissions | K222351 |
| Product codes | BTT |
| Device names | BTT - Humidifier, Respiratory Gas, (Direct Patient Interface) |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5450 |
| Review panels | Anesthesiology |
| Registered establishments | VINCENT MEDICAL(DONGGUAN)TECHNOLOGY COMPANY LIMITED |
| Establishment registrations | 3017235290 |
| FEI numbers | 3017235290 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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