BEUDAMED
    15 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 10, 2013

    ISOFLEX S

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

    SELECT SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·April 12, 2011

    DIMENSION XPAND PLUS WITH HM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·September 5, 2018

    Z NAIL CMF 10.5 X 90 LAG SCR

    FDA Adverse Event
    Malfunction ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HWC·December 6, 2021

    Z NAIL CMF 10MMX17.5CM 125L

    FDA Adverse Event
    Malfunction ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HWC·December 6, 2021

    Z NAIL CMF 10.5 X 90 LAG SCR

    FDA Adverse Event
    Malfunction ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·December 1, 2021

    Z NAIL CMF 13MMX21.5CM 130 L

    FDA Adverse Event
    Malfunction ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·December 1, 2021