Devices

VARiS Version 6.6

Model / Serial
H462074, H462000, H462003, H462004, H462005, H462006, H462011, H462012, H462013, H462014, H462015, H462016, H462017, H462018, H462019, H462020, H462021, H462022, H462023, H462024, H462025, H462026, H462027, H462028, H462029, H462031, H462040, H462045, H462047, H462048, H462049, H462050, H462051, H462052, H462054, H462055, H462057, H462059, H462060, H462061, H462064, H462065, H462066, H462067, H462068, H462072, H462073, H462075, H462076, H462077, H462079, H462082, H462083, H462084, H462085, H462086, H462087
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
The product was distributed to 34 consignees, located in AZ, CA, MA, MI, NC, PA in the USA, and in Australia, Belgium, Canada, Denmark, Finland, France, Germany, Italy, Lithuania, Spain, Sweden, and the United Kingdom
Product Description
Varis Vision Treatment 6.6/RTP Exchange/Siemens Accelerators
Manufacturer
Varian Medical Systems Oncology Systems
1 Event
- Recall of VARiS Version 6.6

Manufacturer

Varian Medical Systems Oncology Systems

Manufacturer Address
Varian Medical Systems Oncology Systems, 911 Hansen Way, Palo Alto CA 94304-1028
Manufacturer Parent Company (2017)
Varian Medical Systems Inc
Source
USFDA

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