FDA device listing
CMAX X-ray Table Side Rails (BF787, TAB830) (MG-SD, LC-FE, PM-CM)
FDA device listing 1752771151 · STERIS Corporation
Key facts
| Proprietary names | CMAX X-ray Table Side Rails (BF787, TAB830) (MG-SD, LC-FE, PM-CM) |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 2150060 |
| Product codes | BWN |
| Device names | BWN - Table And Attachments, Operating-Room |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4950 |
| Review panels | General & Plastic Surgery |
| Registered establishments | STERIS Italy S.r.l. |
| Establishment registrations | 3012708860 |
| FEI numbers | 3012708860 |
| 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