BEUDAMED
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    DERMACLEAN X-AM (PROTEIN LABELING CLAIM) EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623799·PEEK Corp Core, Ø14x24mm

    TUBE OCCLUDING FORCEPS

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

    PMAX NEWTRON XS

    FDA 510(k)
    FDA Class 2 ·Dental

    GLOBAL ADVANTAGE HUM HD 48X18

    FDA Adverse Event
    Injury ·3006356043 JOHNSON & JOHNSON MEDICAL (DEPUY - SUZH·Product code KWT·February 21, 2013

    EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·January 14, 2011

    ABBOTT CLINICAL CHEMISTRY ICT CALIBRATOR

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JGS·July 31, 2014