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

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    INTERLINK SYSTEM EXTENSION SET WITH CONTROL-A-FLO-REGULATORY CLEARLINK SYSTEM EXTENSION SET WITH CONTROL-A-FLO-REGULATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Bone cutters

    FDA UDI
    DFS - DIAMON GmbH·04057176148414·DIADOSS cutter

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00812564032287·LIFE LINK BASIN SET

    LARGE CANNULATED SCREWS

    FDA UDI
    Smith & Nephew, Inc.·03596010063892·6.5MM UNIVERSAL CANNULATED SCREW 70MM

    KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    XENON(TM) PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KIT RSV 30 TEST HOSPITAL VERITOR

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 15, 2021

    IDENTITY ADX DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    HEARTMATE II LVAS

    FDA Adverse Event
    Death ·THORATEC CORP.·Product code DSQ·May 10, 2013

    SROM STM ST,36+8L NK, 18X13X160

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code MRA·June 2, 2011

    THINFLAP SYSTEM CROSS-DRIVE, SELF-DRILLING SCREW 1.5X4MM

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code GWO·April 16, 2018