40 results · 47ms · Sources: EU EUDAMED, US FDA

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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