BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS

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

    MODULAR ROTATING HINGE KNEE TIBIAL ROTATING COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IVENT 201 PORTABLE VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·April 9, 2013

    TI PANGEA LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·March 29, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026