BEUDAMED
    23 results · 33ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Other ×

    SEED SELECTION

    FDA Adverse Event
    Other ·NUCLETRON B.V.·Product code JAQ·November 15, 2011

    SIMULIX RADIOTHERAPY SIMULATOR WITH CT EXTENSION

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code KPQ·September 25, 1997

    VAGINAL APPLICATOR SET

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·August 4, 1997

    RING APPLICATOR

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code HGD·August 4, 1997

    SMX/GENERAL

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code KPQ·February 28, 2011

    SIMULATOR HP

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code KPQ·June 27, 2003

    MICROSELECTRON-HDR

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·April 2, 1998

    MICROSELECTRON-HDR

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·April 2, 1998

    MICROSELECTRON-HDR (CLASSIC)

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·April 2, 1998

    ONCENTRA MASTERPLAN

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code MUJ·June 20, 2008

    MICROSELECTRON-HDR

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·April 2, 1998

    MICROSELECTRON-HDR

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·June 26, 1998

    MICROSELECTRON-HDR (MODEL 105.999)

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·March 16, 1999

    CT/MR FLETCHER TANDEM AND OVOID SET

    FDA Adverse Event
    Other ·NUCLETRON BV·Product code JAQ·August 13, 2010

    *

    FDA Adverse Event
    Other ·*·Product code JAQ·December 27, 2006

    MICROSELECTRON HDR MODEL 105.999

    FDA Adverse Event
    Other ·NUCLETRON B.V.·Product code JAQ·October 15, 2003

    *

    FDA Adverse Event
    Other ·NUCLETRON B.V.·Product code JAQ·October 15, 2003

    PLATO BPS

    FDA Adverse Event
    Other ·NUCLETRON B.V.·Product code MUJ·July 30, 2004

    THERAPLAN PLUS

    FDA Adverse Event
    Other ·NUCLETRON B.V.·Product code MUJ·April 27, 2004

    OCEANTRA MASTERPLAN

    FDA Adverse Event
    Other ·NUCLETRON, B.V.·Product code JAQ·December 23, 2011