BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    MindMotionPRO

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    31P/1H HEAD COIL 3T; 23NA/1H HEAD COIL 3T; 13C/1H HEAD COIL 3T

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION: TO DEPUY DELTA CERAMIC FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 18, 2018

    PURITAN BENNETT 980 SERIES VENTILATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·October 24, 2019

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 11, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 14, 2011

    RECOVERY CONE REMOVAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code GAE·September 8, 2008

    QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests

    FDA Enforcement
    Class II ·Ongoing·Quidel Corporation·May 1, 2024