BEUDAMED
    19 results · 37ms · 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 FDA Adverse Event ×

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Product code NPZ·March 27, 2013

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Product code NPM·March 28, 2013

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 17, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    EQUIMATRIX CANCELLOUS (8503-06-0025)

    FDA Adverse Event
    Injury ·Product code DZE·December 18, 2015

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 15, 2014

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 1, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 26, 2012