BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    CARESIDE ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993634·anteriors; shade BL4; mould BOL

    APR II HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFIED STERILIZATION OF TUR APRONS

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

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 7, 2013

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES, INC.·Product code FTM·July 28, 2014

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·January 6, 2011

    9MM/125 DEG TI CANN TFNA 340MM/LEFT - STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·April 27, 2018

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015