FDA device listing
2026030, 2026035,2026310, 2026000, 2060310, 5025000, 5025310, 5026000,2310000,5191850, 5194850
FDA device listing 1880523632 · INTERSURGICAL UAB
Key facts
| Proprietary names | 2026030, 2026035,2026310, 2026000, 2060310, 5025000, 5025310, 5026000,2310000,5191850, 5194850 |
|---|---|
| Owner/operator | INTERSURGICAL UAB |
| Owner/operator number | 9058058 |
| Product codes | BTT, BZE |
| Device names | BTT - Humidifier, Respiratory Gas, (Direct Patient Interface), BZE - Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5270, 868.5450 |
| Review panels | Anesthesiology |
| Registered establishments | UAB Intersurgical, UAB INTERSURGICAL |
| Establishment registrations | 3001313714, 3021039857 |
| FEI numbers | 3002807293, 3021039857 |
| Establishment operations | Contract 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