BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Impella CP Introducer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CURAD COMPRESSION HOSIERY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEODENT IMPLANT FOR ORTHODONTIC ANCHORAGE

    FDA 510(k)
    FDA Class 2 ·Dental

    PREMIUM PLUS CEEA 28 INSTR. W/TILT-TOP

    FDA Adverse Event
    Injury ·PONCE - USS·Product code GDW·October 8, 2008

    ULTRASONIC IMAGING CATHETER - CORONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·June 27, 2013

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 5, 2011

    PROAQT SENSOR

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code DXG·August 18, 2025

    PROAQT SENSOR

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code DXG·August 18, 2025

    INSTINCT PLUS ENDOSCOPIC CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code PKL·September 16, 2021