BEUDAMED
    8 results · 21ms · 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 ×

    K041492

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 18, 2021

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 4, 2013

    SUPER SHEATH INTRODUCER SHEATH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DRE·December 29, 2010

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 17, 2014

    AMPLATZER® DUCT OCCLUDER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MAE·December 9, 2021

    AMPLATZER® VASCULAR PLUG (UNKNOWN)

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code KRD·December 9, 2021

    FAST-CATH INTRODUCER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DYB·May 21, 2021

    TRANSSEPTAL NEEDLE, BRK SERIES

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DRC·May 21, 2021