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

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    ORGENTEC ANTI-CARDIOLIPIN SCREEN ELISA ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111401033·PLAST LOCKING FCP DA 5 INCHES PK/100

    SURGICAL VITEX

    FDA 510(k)
    FDA Class 2 ·Dental

    Air-Powered Handpieces and Handpiece Attachments

    FDA 510(k)
    FDA Class 1 ·Dental

    PLUM XLM W/DATAPORT

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 11, 2014

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·December 22, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 15, 2013

    IMMULITE 2000 ESTRADIOL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024

    REF H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016

    IMMULITE 2000 ESTRADIOL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024

    IMMULITE 2000 ESTRADIOL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CHP·December 6, 2024