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

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    NXSTAGE PUREFLOW SL

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

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235930·INSTRUMENT 7080919 SCREW REMOVAL TOOL

    BD ANGIOCATH PLUS¿ I.V. CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·September 8, 2022

    MALE NATURAL RUBBER LATEX CONDOM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    128 CHANNEL EEG HEADBOX, MODEL EX-NW-128

    FDA 510(k)
    FDA Class 2 ·Neurology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 26, 2013

    CARPENTIER-EDWARDS PERIMOUNT AORTIC PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 7, 2011

    CORE INTRA-ORAL BLADE

    FDA Adverse Event
    Injury ·STRYKER IRELAND LTD., INSTRUMENTS DIVISION·Product code GFA·July 22, 2008