BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    MRCAT Pelvis

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VERITOR¿ SARS-COV-2 AND FLU A+B

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QMN·October 13, 2021

    INFINITY NELLCOR OXIMAX SMARTPOD, MODEL MS23997

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MESO WOUND MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 4 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 2, 2019

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 17, 2014

    STERNAL ZIPFIX W/NEEDLE PEEK SINGLE PACK

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code JDQ·June 21, 2013

    TURBO ELITE

    FDA Adverse Event
    Malfunction ·SPECTRANETICS CORP·Product code MCW·July 6, 2011

    HAMMER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code LXH·February 11, 2020

    BD VERITOR¿ SARS-COV-2 AND FLU A+B

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QMN·October 27, 2021

    HAMMER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·February 11, 2020