FDA device listing
BF683M ST,BF683M TD,KL100,KL200,Mechanical Table
FDA device listing 1474314641 · Barrfab Industria Comercio Importacao de Equipamentos Hospit
Key facts
| Proprietary names | BF683M ST,BF683M TD,KL100,KL200,Mechanical Table |
|---|---|
| Owner/operator | Barrfab Industria Comercio Importacao de Equipamentos Hospit |
| Owner/operator number | 10042376 |
| Product codes | FWX |
| Device names | FWX - Table, Operating-Room, Mechanical |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4950 |
| Review panels | General & Plastic Surgery |
| Registered establishments | BARRFAB INDUSTRIA COMERCIO IMPORTACAO DE EQUIPAMENTOS HOSPIT |
| Establishment registrations | 3006467297 |
| FEI numbers | 3006467297 |
| Establishment operations | 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