BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    PROFORM GENERAL APPLICATION CEMENTED FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970490·anteriors; shade BL1; mould UIL

    Celesteion, PCA-9000A/3

    FDA 510(k)
    FDA Class 2 ·Radiology

    CIRQLATOR INTRATHORACIC PRESSURE REGULATOR (ITPR)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LEAD EXTRACTION LIBERATOR BEACON TIP LOCKING STYLET

    FDA Adverse Event
    Injury ·COOK VANDERGRIFT INC·Product code DRB·April 14, 2021

    ARTHREX AR-9704-90

    FDA Adverse Event
    Injury ·MEDISISS·Product code GEI·November 11, 2009

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·June 29, 2017

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013

    SOLAR 8000M

    FDA Adverse Event
    Injury ·GE HEALTHCARE·Product code MHX·January 20, 2011

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 31, 2014