BEUDAMED
    9 results · 16ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    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

    SELECT SHOULDER COGR HUMERAL HEAD 52 X 26

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

    28MM COCR MOD HD +6MM NO SKIRT

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

    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

    3M FLUID RESISTANT FACE MASK

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

    PALMAZ SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS, A JOHNSON AND JOHNSON CO·Product code MAF·April 15, 1998

    IMPL TAPERED SCR-V SBM 6M M 5.7MM 10MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·July 19, 2019