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

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    MobileECG 2 BT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WATERLASE MD TURBO PLUS MODEL 7200XXX

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

    POWDER-FREE VINYL EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 27, 2011

    ALTRX +4 10D 36IDX56OD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 21, 2013

    EDWARDS MC3 TRICUSPID ANNULOPLASTY SYSTEM

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·September 29, 2008

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·June 15, 2025

    Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971

    FDA Enforcement
    Class II ·Terminated·ArthroCare Corporation·September 30, 2020