FDA device listing
27 Touchdisplay Foreseeson,Barco Display,MDSC-2226, MDSC-2232, MDSC-2242, MDSC-2324, MDSC-2326, MDSC-8231, MDSC-8255…
FDA device listing 1461137459 · Brainlab SE
Key facts
| Proprietary names | 27 Touchdisplay Foreseeson,Barco Display,MDSC-2226, MDSC-2232, MDSC-2242, MDSC-2324, MDSC-2326, MDSC-8231, MDSC-8255, MDSC-8258, MDSC-8527NXF M2, MDSC-8532NXF M2 |
|---|---|
| Owner/operator | Brainlab SE |
| Owner/operator number | 9004547 |
| Product codes | KQM |
| Device names | KQM - Camera, Surgical And Accessories |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4160 |
| Review panels | General & Plastic Surgery |
| Registered establishments | BRAINLAB SE |
| Establishment registrations | 8043933 |
| FEI numbers | 3002619595 |
| Establishment operations | Foreign Exporter |
| 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