U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Accelerator, linear, medical - Product Code IYE
원인
If "confirm" or "unconfirm" settings are clicked during the "terminated checking" phase of treatment delivery, desktop pro cancels the loaded beam and sets the beam mus to zero. desktop pro then sends the delivered mus to mosaiq a a zero value.
조치
Elekta sent an IMPORTANT NOTICE letter dated March 9, 2011 to affected customers. The notice identified the product, the problem, and the corrective action to be taken by the customer. The notice advise all customers to follow any instructions or recommendations covered in the Notice. For questions call +44(0)1293 654200.
Nationwide Distribution (USA) including the states of: AZ, CA, GA, IL, LA, MD, MA, MI, MN, NJ, NY, NC, OH, PA, TN, VA, WI and Puerto Rico
제품 설명
Elekta Synergy XVI 4.5 || Product Usage: Radiation therapy treatment of malignant neoplastic diseases, as determined by a licensed medical practitioner.