BEUDAMED
    213 results · 26ms · Sources: EU EUDAMED, US FDA

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    PROPOSED OPTIMUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ATRIUM GRADUATED WALL FLIXENE AX-BIFEM GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STURDY MANUAL RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 12, 2015

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    CAIMAN DISP. INSTR. ARTICULAR D-12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·May 6, 2014

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL S.A.·Product code GEI·March 21, 2014

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 7, 2026

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 3, 2026

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·June 10, 2011

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 22, 2008

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·April 30, 2026