BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SYNTHES (USA) DISTAL RADIUS PLATE SYSTEM (DRPS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: CAPSTONE SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JTL-250-01

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

    AXIOM ARISTOS VX PLUS

    FDA Adverse Event
    Injury ·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD·Product code MQB·April 7, 2021

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 25, 2013

    NAIL

    FDA Adverse Event
    Injury ·SMITH-NEPHEW INC.·Product code JDS·February 9, 2011

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 24, 2014