BEUDAMED
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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749105391·CERAMO-S PLANO vessel scissors, angl. 140°, 190 mm

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749009682·CERAMO TC RONDO micro vessel scissors, 0°, 210 mm

    POWERFLEX P3 4MM X 4CM, 135CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·September 20, 2004

    POWERFLEX P3 4MM X 4CM, 136CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·September 20, 2004

    SAVVY PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code LIT·September 30, 2011

    POWERFLEX P3 5MM X 4CM, 135CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·May 3, 2005

    PALMAZ GENESIS AMIIA

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·February 27, 2012

    ZILVER PTX DRUG-ELUTIN PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MAF·February 11, 2013

    SLALOM PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code LIT·December 14, 2011

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MAF·February 11, 2013

    POWERFLEX P3 6MM X 4CM, 40CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·November 24, 2004

    STERLING

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·November 9, 2023

    PRECISE PRO RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code NIM·December 16, 2014

    POWERFLEX P3 4MM X 4CM, 135CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·December 9, 2004

    PTA SAVVY 2.0X4CM 120CM

    FDA Adverse Event
    CORDIS EUROPA, N.V.·Product code LIT·October 13, 2004

    PTA AMIIA, 5.0 X 40MM, 142CM

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·October 22, 2004

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·February 21, 2013

    PALMAZ GENESIS UNKNOWN

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·August 11, 2011

    AVIATOR PLUS PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code LIT·August 11, 2011

    PALMAZ XL STENT PER 40MM UNMOUNTED

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·December 11, 2014