BEUDAMED
    10,000 results · 68ms · 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 ×

    CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS CORP·Product code NIQ·December 5, 2003

    CORDIS CORPORATION

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION/QUALITY CONTROL·Product code DYB·February 28, 2003

    CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DQX·June 20, 1997

    CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS CORP.·Product code DQX·October 1, 2002

    UNK - PRODUCT - CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS US. CORP·Product code DYB·February 20, 2023

    UNK - PRODUCT - CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS US. CORP·Product code DQX·December 26, 2022

    UNK - PRODUCT - CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS US. CORP·Product code DQX·December 22, 2022

    UNK - PRODUCT - CORDIS CORPORATION

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code LIT·August 9, 2022

    JOHNSON & JOHNSON CORDIS CORPORATION

    FDA Adverse Event
    Malfunction ·CORDIS CORP·Product code MAF·July 10, 1997

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKVISTABRITEC

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DQY·February 15, 2019

    UNKNOWN PTA

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code LIT·February 15, 2019

    12K HAND CONTROL SHAVER HANDPIECE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code HRX·February 5, 2010

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 20, 2006

    FIRE STAR RX PTCA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code LOX·January 31, 2008

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 19, 2006

    PALMAZ XL STENT PER 40 MM OUS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·February 9, 2010