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

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    ATRAUMATIC SPECIAL SPROTTE NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526780736·LEVAMED ACTIVE ANKLE SUP SLVR L I

    PAQ. 112x100x146 CTG TRISMED FM 800G

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763084372·

    Epimed

    FDA UDI
    EPIMED INTERNATIONAL, INC·00818788021540·Nexus™ Epidural Catheter Connector 21g

    PRISMA HF 1000 SET, PRISMA HF 1000 PRE-SET

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

    MISSION U500 URINE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Hematology

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 5, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 18, 2012

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 29, 2015

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 8, 2017

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 14, 2012

    CE INTERMATE XLV 250, 12 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·November 30, 2010

    UNIDENTIFIED ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 2, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·December 14, 2012