BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BARD® TIEMANN MODEL UROLOGICAL CATHETER COUDE TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·September 15, 2023

    BARD® TIEMANN MODEL UROLOGICAL CATHETER COUDE TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·July 14, 2025

    BARD® TIEMANN MODEL UROLOGICAL CATHETER COUDE TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·July 14, 2025

    BARDAM COUDE CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·September 16, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·February 11, 2011

    CALAXO - UNK

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code HWC·March 10, 2008

    BARD® TIEMANN MODEL UROLOGICAL CATHETER COUDE TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·July 7, 2025

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·September 16, 2021