BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    MODEL #M8 ELECTRONIC STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    3M™ Unitek™

    FDA UDI
    3M COMPANY·30605861028654·3M™ Unitek™ Stainless Steel Second Permanent Mo...

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981129316·Conical Reamer, Tri-Flat

    TCP

    FDA UDI
    WRIGHT MEDICAL TECHNOLOGY, INC.·00840420118844·

    RESPONSE 2000 CEMENTED HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEMORPEX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SNAP-RING FOR 52MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 4, 2007

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NDN·March 14, 2018

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 6, 2014

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 7, 2013

    TAUT ADAPTOR - BARIATRIC PORT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GCJ·October 27, 2010

    SPIRAL BLADE INSERTER FOR HINDFOOT ARTHRODESIS NAIL-EX

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code FZX·November 24, 2015