FDA device listing
MULTIX Impact E
FDA device listing 1158493037 · Siemens Healthineers AG
Key facts
| Proprietary names | MULTIX Impact E |
|---|---|
| Owner/operator | Siemens Healthineers AG |
| Owner/operator number | 8010024 |
| Premarket submissions | K220919 |
| Product codes | KPR, MQB |
| Device names | KPR - System, X-Ray, Stationary, MQB - Solid State X-Ray Imager (Flat Panel/Digital Imager) |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1680 |
| Review panels | Radiology |
| Registered establishments | Siemens Healthineers AG, SIEMENS SHANGHAI, MEDICAL EQUIPMENT LTD. |
| Establishment registrations | 3003202425, 3004977335 |
| FEI numbers | 3003202425, 3004977335 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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