BEUDAMED
    26 results · 35ms · Sources: EU EUDAMED, US FDA

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    P-Cure Proton Beam Therapy System

    FDA 510(k)
    FDA Class 2 ·Radiology

    BE PLUS LTM AMPLIFIER GWI AMPLIFIER

    FDA 510(k)
    FDA Class 2 ·Neurology

    BOLTON PTA CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTHES ANTERIOR CERVICAL PLATE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JDN·May 21, 1997

    CAPTURE-R READY INDICATOR RED CELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR·Product code KSZ·May 18, 2007

    TRIMPORT IMPLANTABLE VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    GERARD MEDICAL, INC.·Product code LJT·June 6, 1997

    VENTAK MINI+ IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·March 6, 1997

    ZYPLAST COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·October 10, 1997

    VENTAK MINI+ IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

    SELECT SHOULDER COGR HUMERAL HEAD 52 X 26

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code HSD·August 22, 1997

    TRIMPORT IMPLANTABLE VASCULAR

    FDA Adverse Event
    Malfunction ·GERARD MEDICAL, INC.·Product code LJT·October 2, 1997

    VALLEYLAB ELECTROSURGICAL GENERATOR

    FDA Adverse Event
    Malfunction ·VALLEYLAB, INC.·Product code GEI·July 24, 1998

    CAPTURE-R READY-ID TEST WELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 11, 2007

    28MM COCR MOD HD +6MM NO SKIRT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·January 30, 2015

    EXTENSION TUBE, 10 CM LENGTH, 15F/15M

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC SPA·Product code CAH·December 9, 1996

    28MM MOD HD STD NECK TP1 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·January 30, 2015

    ULTRA-THIN BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code LIT·November 6, 2008

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 17, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 5, 2013

    3M FLUID RESISTANT FACE MASK

    FDA Adverse Event
    Injury ·3M MEDICAL PLANT·Product code FXX·August 6, 1997