FDA device listing
Arrow1600 (VB) - Arrow Central Venous Catheter,Arrow1600 (VB) - Arrowg+ard Blue Central Venous Catheter
FDA device listing 1569940653 · STERIS Corporation
Key facts
| Proprietary names | Arrow1600 (VB) - Arrow Central Venous Catheter,Arrow1600 (VB) - Arrowg+ard Blue Central Venous Catheter |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10042227 |
| Product codes | FOZ |
| Device names | FOZ - Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5200 |
| Review panels | General Hospital |
| Registered establishments | STERIS AST CZ s.r.o. |
| Establishment registrations | 3004784537 |
| FEI numbers | 3004784537 |
| 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