BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    SDU 500 DIAGNOSTIC ULTRASOUND INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756352055·DR DILLIN SCOPE PACK

    STEM: AMISTEM-P COLLARED STD. SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 5, 2021

    DYNA-EXTOR II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROPORT PLASTIC VENOUS IMPLANTABLE ACCESS SYSTEMS PRE-ASSEMBLED WITH SILICONE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACTIVA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·January 11, 2013

    SECUR-FIT MAX

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·November 23, 2010

    RESTORE PRIME

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 2, 2014