FDA device listing
Servo Humidifier 161,Servo Humidifier 162,Servo Humidifier 163,Servo Humidifier 172,Servo Humidifier 173
FDA device listing 1940431674 · Maquet Critical Care AB
Key facts
| Proprietary names | Servo Humidifier 161,Servo Humidifier 162,Servo Humidifier 163,Servo Humidifier 172,Servo Humidifier 173 |
|---|---|
| Owner/operator | Maquet Critical Care AB |
| Owner/operator number | 8010042 |
| Product codes | BYD |
| Device names | BYD - Condenser, Heat And Moisture (Artificial Nose) |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5375 |
| Review panels | Anesthesiology |
| Registered establishments | MAQUET CRITICAL CARE AB |
| Establishment registrations | 8010042 |
| FEI numbers | 3002808128 |
| 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