BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    HYBRID CAPTURE II GC-ID

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981485·anteriors; shade BL2; mould US2

    SOMNOWATCH

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    EPIQ , EPIQ 5, EPIQ 7, Affiniti 30, Affiniti 50 and Affiniti 70 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ECHELON*FLEX60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 27, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MED SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·February 1, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·August 5, 2014

    EPIQ 7C ULTRASOUND CHINA LOCAL

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND (SHANGHAI) CO., LTD·Product code IYN·June 2, 2023

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 14, 2015