FDA device listing
ET TUBE SHER-I-BRONCH LS 28 FR,ET TUBE SHER-I-BRONCH LS 35 FR,ET TUBE SHER-I-BRONCH LS 37 FR,ET TUBE SHER-I-BRONCH LS 39…
FDA device listing 1956238670 · Sotera Health LLC
Key facts
| Proprietary names | ET TUBE SHER-I-BRONCH LS 28 FR,ET TUBE SHER-I-BRONCH LS 35 FR,ET TUBE SHER-I-BRONCH LS 37 FR,ET TUBE SHER-I-BRONCH LS 39 FR,ET TUBE SHER-I-BRONCH LS 41 FR,Sher-I-Bronch Endobronchial Tube |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | CBI |
| Device names | CBI - Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5740 |
| Review panels | Anesthesiology |
| Registered establishments | Sterigenics US LLC |
| Establishment registrations | 1423662, 3004111573 |
| FEI numbers | 3000215273, 3004111573 |
| Establishment operations | Contract Sterilizer |
| 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