FDA device listing
VerathonMedical5877 (WT) - GlideScope AVL Single Use,VerathonMedical5877 (WT) - GlideScope GVL Single…
FDA device listing 1291798806 · STERIS Corporation
Key facts
| Proprietary names | VerathonMedical5877 (WT) - GlideScope AVL Single Use,VerathonMedical5877 (WT) - GlideScope GVL Single Use,VerathonMedical5877 (WT) - GlideScope Ranger Single Use |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 1527821 |
| Product codes | CCW |
| Device names | CCW - Laryngoscope, Rigid |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5540 |
| Review panels | Anesthesiology |
| Registered establishments | Isomedix Operations, Inc., STERIS Applied Sterilization Technologies ULC |
| Establishment registrations | 2030624, 9680143 |
| FEI numbers | 3000206435, 3002807308 |
| 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