BEUDAMED
    43 results · 23ms · Sources: EU EUDAMED, US FDA

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    MIDAS TOUCH NITRILE EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964001589·The ENDO CARRY-ON Procedure Kit contains all of...

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741042713·Catheter Placement Kit

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014603353·A-Line Positioner with Straps

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167900001430·

    Patient Cable

    FDA UDI
    GLOBAL INSTRUMENTATION, LLC·90815187020061·Patient Cable 5L IEC

    GAS MODULE II, MODEL 0998-00-0143

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CURE LP

    FDA UDI
    SpineArt SA·07640270060675·ANTERIOR LUMBAR PLATE L43

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1900001430·

    DRG AURICA ELISA TESTOSTERONE KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AVL OPTI R ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·February 16, 2022

    RUBY COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·January 4, 2016

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 12, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHECARE·Product code MKJ·February 18, 2011

    ACCU-CHEK ADVANTAGE II TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code NBW·February 19, 2008

    RIGIFLEX II ACHALASIA DILATATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORK, LTD·Product code KNQ·October 24, 2007

    DIMENSION®

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·March 8, 2018

    DIMENSION®

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·March 8, 2018

    DIMENSION®

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·March 8, 2018