BEUDAMED
    25 results · 26ms · Sources: EU EUDAMED, US FDA

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    BILOX PROSTHESIS HEAD 12/14 28MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·May 23, 2014

    MODIFICATION TO: METHA HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    BIOLOX PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B582083495·AWL

    ACCU-CHEK ® ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 4, 2015

    ACCU-CHEK ® ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 4, 2015

    ACCU-CHEK ® ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 4, 2015

    WELCH ALLYN VITALS SOFTWARE DEVELOPERS KIT (SDK)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANCURE LLIAC BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK ® ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 4, 2015

    ACCU-CHEK ® FLEXLINK INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 2, 2015

    ACCU-CHEK ® FLEXLINK INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 2, 2015

    ACCU-CHEK ® FLEXLINK INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·June 2, 2015

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 29, 2013

    MAXCEM ELITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·May 10, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·July 28, 2008