FDA device listing
22M-22M/15F Straight Connector CircuitLife,Breathing Circuit 180cm SB, Whisper Connector CircuitLife,Double Swivel…
FDA device listing 1015943211 · CircuitLife LLC
Key facts
| Proprietary names | 22M-22M/15F Straight Connector CircuitLife,Breathing Circuit 180cm SB, Whisper Connector CircuitLife,Double Swivel Connector Open 15M-15F/22M CircuitLife,Double Swivel Elbow Connector Closed CircuitLife,Elbow Connector 22M/15F-15M/22F CircuitLife,Exhalation Valve Connector,Exhalation Valve Connector with port,Straight CO2 Exhalation Connector - No swivel,T adapter with one-way valve,Whisper… |
|---|---|
| Owner/operator | CircuitLife LLC |
| Owner/operator number | 10062691 |
| Product codes | BZA |
| Device names | BZA - Connector, Airway (Extension) |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5810 |
| Review panels | Anesthesiology |
| Registered establishments | CIRCUITLIFE LLC |
| Establishment registrations | 3016634999 |
| FEI numbers | 3016634999 |
| Establishment operations | Repackager/Relabeler |
| 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