BEUDAMED
    36 results · 19ms · Sources: EU EUDAMED, US FDA

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    HUDSON RCI

    FDA Adverse Event
    Other ·REAVEN PANGAL PK·Product code CAT·January 30, 2008

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    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FPK·November 10, 2008

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FPK·March 5, 2007

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FPK·November 10, 2008

    CELL-DYN 1700

    FDA Adverse Event
    Other ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code JPK·February 23, 2006

    CELL-DYN 1700

    FDA Adverse Event
    Other ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code JPK·February 23, 2006

    PATIENT ADMIN. SET FOR USE WITH THE

    FDA Adverse Event
    Other ·BRACCO DIAGNOSTICS INC.·Product code FPK·August 25, 2014

    CELL DYN SAPPHIRE ANALYZER

    FDA Adverse Event
    Other ·ABBOTT LABORATORIES DIVISION/CELLDYN·Product code JPK·October 25, 2006

    OLYMPUS INJECTION TUBE

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FPK·October 23, 2012

    CELL-DYN 16 TRI-LEVEL CONTROL

    FDA Adverse Event
    Other ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code JPK·March 25, 1997

    SONOPET OMNIULTRASONIC DISPOSABLE TUBING KIT

    FDA Adverse Event
    Other ·SYNRGETICS·Product code FPK·August 6, 2007

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FPK·July 3, 2008

    9610617-2008-00015

    FDA Adverse Event
    Other ·Product code FPK·July 3, 2008

    9610617-2008-00016

    FDA Adverse Event
    Other ·Product code FPK·July 12, 2008

    CELL-DYN 16 TRI-LEVEL CONTROL

    FDA Adverse Event
    Other ·ABBOTT DIAGNOSTIC DIVISION/CELLDYN·Product code JPK·May 24, 2002

    1310P MEDITRACE 2/PK 20/CA

    FDA Adverse Event
    Other ·COVIDIEN·Product code MLN·May 11, 2012

    1310P MEDITRACE 2/PK 20/CA

    FDA Adverse Event
    Other ·COVIDIEN·Product code DRX·March 25, 2013

    1310P MEDITRACE 2/PK 20/CA

    FDA Adverse Event
    Other ·COVIDIEN·Product code MLN·January 18, 2013

    1310 EDITRCE 2/PK 20/CA

    FDA Adverse Event
    Other ·TYCO HEALTHCARE·Product code LDD·May 12, 2005

    1310P MEDITRACE 2/PK 20/CA

    FDA Adverse Event
    Other ·TYCO HEALTHCARE·Product code LDD·May 12, 2005