BEUDAMED
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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749121124·CERAMO HCR micro non-traum. forceps,str. double...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749105094·CERAMO HCR knot pusher 25° angl., 340 mm, d=3mm

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749105100·CERAMO HCR knot pusher 25° angl., 280 mm, d=3mm

    MODIFIED MSQ FAMILY OF LOVELY LIGHT/LASER SYSTEMS

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

    PRECISE SERIES LINAC

    FDA Adverse Event
    Malfunction ·ELEKTA LTD·Product code IYE·May 13, 2016

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 21, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 21, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 22, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 21, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 21, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 21, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 22, 2018

    SONATA SYSTEM LASER (MYTHOS 500)

    FDA Adverse Event
    Malfunction ·MSQ (M2) LTD.·Product code GEX·June 21, 2004

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·August 22, 2025

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·November 21, 2018

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code IYE·May 13, 2020

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES, INC·Product code LWR·April 4, 2008

    ELEKTA SYNERGY

    FDA Adverse Event
    Malfunction ·ELEKTA LTD·Product code IYE·June 16, 2017

    ELEKTA SYNERGY

    FDA Adverse Event
    Malfunction ·ELEKTA LTD·Product code IYE·June 16, 2017

    ELEKTA SYNERGY

    FDA Adverse Event
    Malfunction ·ELEKTA LTD·Product code IYE·June 16, 2017