BEUDAMED
    4,210 results · 43ms · Sources: EU EUDAMED, US FDA

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    SEA SPINE

    FDA Adverse Event
    Injury ·S1 SPINE·Product code MAX·March 21, 2012

    SEA PORT

    FDA Adverse Event
    Malfunction ·HARBOR MEDICAL·January 14, 1994

    SEA-BOND

    FDA Adverse Event
    Injury ·COMBE INC.·Product code KOL·November 20, 2010

    SEA BROOK

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code ILO·August 10, 1998

    SEA BAND

    FDA Adverse Event
    SEA-BAND, LTD.·Product code MVV·March 3, 2023

    SEA-BOND DENTURE ADHESIVE UPPER WAFERS

    FDA Adverse Event
    Injury ·COMBE INCORPORATED·Product code KXW·March 4, 2010

    FLEXI-SEA FMS

    FDA Adverse Event
    Injury ·CONVATEC·Product code KNT·December 10, 2010

    UNKNOWN SEAS AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDB·March 1, 2018

    UNKNOWN SEAS HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·February 28, 2018

    SEA-BOND WAFERS

    FDA Adverse Event
    Injury ·Product code KXX·September 27, 2013

    SUPER POLIGRIP CREAM

    FDA Adverse Event
    Other ·GLAXOSMITHKLINE·Product code KOL·April 27, 2009

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 9, 2009

    3MM DRIVER LARGE AXIAL DRIVER

    FDA Adverse Event
    Malfunction ·SEA SPINE, INC.·Product code MAX·February 18, 2014

    OLYMPUS FLUSHING PUMP

    FDA Adverse Event
    Other ·SOUTHEND-ON-SEA·Product code FEQ·April 10, 2009

    HYPERBARIC CHAMBER 31"

    FDA Adverse Event
    Malfunction ·SUMMIT TO SEA·Product code CBF·March 14, 2018

    SEA MED PACING SYSTEM ANALYZER

    FDA Adverse Event
    Death ·SEA MED CORP.·Product code DTC·February 19, 1998

    HYPERBARIC CHAMBER 40"

    FDA Adverse Event
    Injury ·SUMMIT TO SEA·Product code CBF·January 13, 2022

    BIOTENE MOUTHWASH (2013 FORMULATION)

    FDA Adverse Event
    Injury ·KIK CUSTOM PRODUCTS·Product code LFD·November 13, 2018

    BASIC CONFIGURATION MODEL 6500

    FDA Adverse Event
    Other ·STRYKER MEDICAL·Product code FPO·June 17, 2011

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 6, 2025