FDA device listing
Non-winged Tuohy,Perican Tuohy,Perifix,Perifix Tuohy
FDA device listing 1668626643 · B. BRAUN MEDICAL INDUSTRIES SDN. BHD.
Key facts
| Proprietary names | Non-winged Tuohy,Perican Tuohy,Perifix,Perifix Tuohy |
|---|---|
| Owner/operator | B. BRAUN MEDICAL INDUSTRIES SDN. BHD. |
| Owner/operator number | 8040308 |
| Product codes | CAZ |
| Device names | CAZ - Anesthesia Conduction Kit |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5140 |
| Review panels | Anesthesiology |
| Registered establishments | B. BRAUN MEDICAL INDUSTRIES SDN. BHD. |
| Establishment registrations | 9612086 |
| FEI numbers | 3002806575 |
| Establishment operations | Contract 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