FDA device listing
Astra-Vue,Astra-Vue ALTIS,Astra-Vue LITE,Astra-Vue PRO,Astra-Vue ULTRA
FDA device listing 1564533915 · Goldstar Medical Instruments
Key facts
| Proprietary names | Astra-Vue,Astra-Vue ALTIS,Astra-Vue LITE,Astra-Vue PRO,Astra-Vue ULTRA |
|---|---|
| Owner/operator | Goldstar Medical Instruments |
| Owner/operator number | 9053992 |
| Product codes | CCW |
| Device names | CCW - Laryngoscope, Rigid |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5540 |
| Review panels | Anesthesiology |
| Registered establishments | GOLDSTAR MEDICAL INSTRUMENTS |
| Establishment registrations | 3000126234 |
| FEI numbers | 3000126234 |
| Establishment operations | Contract Manufacturer, 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