BEUDAMED
    9 results · 18ms · 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: Injury ×

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·May 8, 2008

    INFUSE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 11, 2011

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 12, 2011

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 12, 2011

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 12, 2011

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·April 27, 2021

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code MFE·November 19, 2021

    REFLEX CATHETER

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code DQY·November 19, 2021

    MARATHON

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. EV3 NEUROVASCULAR·Product code KRA·November 19, 2021