40 results
·
47ms
·
Sources: EU EUDAMED, US FDA
Vision RT Ltd.
Manufacturer
6 Basic UDI-DIs·8 Devices·3 Importers
Vision RT Ltd
FDA registration
Vision RT Ltd·2 products·🇬🇧 United Kingdom
Patient ID
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market·32 countries
VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - OTHER
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market
VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - HARDWARE ACCESSORIES
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market
VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - HARDWARE ACCESSORIES
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market
Real-Time Coach
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market·32 countries
SafeID
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market·9 countries
SafeID Kiosk
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market·10 countries
SafeID
Device
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·On the market·12 countries
ALIGNRT
FDA Adverse Event
Malfunction
·VISION RT LTD·Product code IYE·October 22, 2014
ALIGNRT PLUS
FDA Adverse Event
Malfunction
·VISION RT LTD.·Product code IYE·August 11, 2021
ALIGNRT PLUS
FDA Adverse Event
Malfunction
·VISION RT LTD·Product code IYE·July 13, 2021
ALIGNRT
FDA Adverse Event
Malfunction
·VISION RT LTD·Product code IYE·December 18, 2013
ALIGNRT
FDA Adverse Event
Malfunction
·VISION RT LTD·Product code IYE·December 18, 2013
AlignRT Plus [private label-OSMS] K123371: The AlignRT Plus system is indicated for use to position and monitor patients relative to the prescribed treatment isocentre, and to withhold the beam automatically during radiation delivery.
FDA Recall
Terminated
·Vision RT Ltd Dove House, Arcadia Avenue London United Kingdom·Product code IYE·June 30, 2016
TrueBeam Radiotherapy Delivery System and EDGE" Radiotherapy Delivery System, K140528. The TrueBeam and Edge Systems are intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation therapy is indicated for adults and pediatric patients.
FDA Recall
Terminated
·Vision RT Ltd Dove House, Arcadia Avenue London United Kingdom·Product code IYE·June 30, 2016
GATERT
FDA Adverse Event
Malfunction
·ION RT LTD., VISION RT LIMITED·Product code IYE·February 9, 2016
Patient ID
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·1 device
DoseRT Camera
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Vision RT Ltd.·1 device