601 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Elekta Inc.
FDA registration
Elekta Inc.·3 products·🇺🇸 United States
Monaco
FDA UDI
ELEKTA, INC.·00858164002046·
Monaco
FDA UDI
ELEKTA, INC.·00858164002183·
Monaco
FDA UDI
ELEKTA, INC.·00858164002268·
MOSAIQ
FDA UDI
ELEKTA, INC.·00858164002091·
XiO
FDA UDI
ELEKTA, INC.·00858164002114·
MOSAIQ
FDA UDI
ELEKTA, INC.·00858164002220·
MOSAIQ
FDA UDI
ELEKTA, INC.·00858164002237·
Monaco
FDA UDI
ELEKTA, INC.·00858164002244·
Monaco
FDA UDI
ELEKTA, INC.·00858164002190·
ERGO Localizer
FDA UDI
ELEKTA, INC.·00858164002213·
Monaco
FDA UDI
ELEKTA, INC.·00858164002169·
Atlas-Based Autosegmentation
FDA UDI
ELEKTA, INC.·00858164002039·
Monaco
FDA UDI
ELEKTA, INC.·00858164002152·
ERGO++
FDA UDI
ELEKTA, INC.·00858164002206·
ELEKTA INC
FDA Adverse Event
Product code IWB·February 3, 2014
MALCOLM RAND PINS
FDA Adverse Event
Injury
·CMI/ELEKTA INSTRUMENTS, INC.·Product code HBL·December 31, 2002
MONACO
FDA Adverse Event
Malfunction
·ELEKTA INC.·Product code MUJ·July 3, 2020
HDR BRACHTHERAPY SYSTEM
FDA Adverse Event
Malfunction
·ELEKTA, INC.·Product code KXK·June 13, 2018
SYNERGY XVI
FDA Adverse Event
Malfunction
·ELEKTA LTD.·Product code IYE·November 19, 2007