Devices

Device Recall ONCOR Impression Plus

Model / Serial
Serial no: 3855 4019 4067 3953 5148 3793 5098 5222 3801 5388 3948 3755 5033 4015 5095
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution- US Nationwide in the states: AL, CA, FL, GA, IL, IN, KY, MA, MI, MO, MS, NJ, NY, OH, OK, PA, RI, SC, TN, TX, WI, WV, and WY; and PR. International distribution to Nassau.
Product Description
ONCOR Impression Plus, Digital Linear Accelerator, Model No. 05857912 || Product Usage: || The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
Manufacturer
Siemens Medical Solutions USA, Inc
1 Event
- Recall of Device Recall ONCOR Impression Plus

Manufacturer

Siemens Medical Solutions USA, Inc

Manufacturer Address
Siemens Medical Solutions USA, Inc, 40 Liberty Blvd, Malvern PA 19355-1418
Manufacturer Parent Company (2017)
Siemens Ag
Source
USFDA

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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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