BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Neo GBR System

    FDA 510(k)
    FDA Class 2 ·Dental

    SYRINGE 0.3ML 8MM 90 BX 450 MO

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·April 23, 2021

    MESA SPINAL SYSTEM (KEYSTONE RODS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMC SURGICAL DRAPE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SYRINGE 0.3ML 8MM 90 BX 450 MO

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 2, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 23, 2014

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·June 16, 2011

    MOZEC¿ NC RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·December 13, 2022

    FMsealer Open Shears. Model FM3001

    FDA Enforcement
    Class II ·Terminated·Domain Surgical, Inc.·December 7, 2016