Devices

Device Recall MEVATRON

Model / Serial
Part number 8317000, all units
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA (nationwide)
Product Description
Mevatron M 6730/6740; || Siemens Healthcare || Concord, CA 94520 || Product Usage: PRIMUS and MEVATRON Linear Accelerators are intended to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.
Manufacturer
Siemens Medical Solutions USA, Inc
2 Events
- Recall of Device Recall MEVATRON
- Recall of Device Recall MEVATRON

Manufacturer

Siemens Medical Solutions USA, Inc

Manufacturer Address
Siemens Medical Solutions USA, Inc, 4040 Nelson Ave, Concord CA 94520-1200
Source
USFDA

52 devices with a similar name

Learn more about the data here

Device Recall MEVATRON M 6700 (MX)

Model / Serial
Device Model Number 5693908 Serial numbers: 3009 2958 2863 2972 2646 3079 2516 2962 3055 1452 2702 2125 3066 2689 2228 2564 2507 1904 3075 2375 3013 3068 2596 3025 3049 2965 2045 3084 2855 2906 2292 2384 2067 2818 3089
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
MEVATRON M 6700 (MX) Accelerator, Linear, Medical || The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall MEVATRON M 6730/6740 (MEX)

Model / Serial
Device Model Number 8319758 Serial numbers: 3009 2958 2863 2972 2646 3079 2516 2962 3055 1452 2702 2125 3066 2689 2228 2564 2507 1904 3075 2375 3013 3068 2596 3025 3049 2965 2045 3084 2855 2906 2292 2384 2067 2818 3089
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
MEVATRON M 7400/7440(MEX) Accelerator, Linear, Medical || The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall MEVATRON M 6730/6740 (MEX)

Model / Serial
Device Model Number 9401654, 9401746, 8490005 Serial numbers: 3009 2958 2863 2972 2646 3079 2516 2962 3055 1452 2702 2125 3066 2689 2228 2564 2507 1904 3075 2375 3013 3068 2596 3025 3049 2965 2045 3084 2855 2906 2292 2384 2067 2818 3089
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
MEVATRON MD-2, MEVATRON MDX-2 and MEVATRON ME, accelerator, Linear, Medical || The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall MEVATRON KD2

Model / Serial
Device Model Number 8515520 Serial numbers: 3009 2958 2863 2972 2646 3079 2516 2962 3055 1452 2702 2125 3066 2689 2228 2564 2507 1904 3075 2375 3013 3068 2596 3025 3049 2965 2045 3084 2855 2906 2292 2384 2067 2818 3089
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution
Product Description
MEVATRON KD-2, accelerator, Linear, Medical || The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Manufacturer
Siemens Medical Solutions USA, Inc

Device Recall Mevatron M2/Primus Mid Energy and PRIMUS HI

Model / Serial
Device Model# 1940035, 4504200
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Distributed throughout the United States
Product Description
Mevatron M2/Primus Mid-Energy || PRIMUS HI
Manufacturer
Siemens Medical Solutions USA, Inc

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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