BEUDAMED
    13 results · 36ms · Sources: EU EUDAMED, US FDA

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    6000039-2001-00055

    FDA Adverse Event
    Injury ·Product code LIT·December 13, 2001

    NAVIGUIDE GUIDE WIRE

    FDA Adverse Event
    Injury ·MEDI-TECH·Product code DQX·July 23, 1998

    NAVIGUIDE GUIDE WIRE

    FDA Adverse Event
    Injury ·MEDI-TECH·Product code DQX·July 23, 1998

    OCCLUSION BALLOON CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH·Product code LIT·July 20, 2000

    OCCLUSION BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·MEDI-TECH·Product code LIT·July 20, 2000

    ARCHITECT IPTH

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code CEW·March 12, 2013

    SOFT-VU ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code DQO·February 18, 2011

    INDURA

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LKK·February 15, 2008

    NUVASIVE COROENT PROCEDURE

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code MQP·April 11, 2013

    GOLVO 8000

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FSA·July 31, 2025

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·September 26, 2007

    SMR REVERSE HUMERAL BODY SHORT

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·March 11, 2022