BEUDAMED
    252 results · 58ms · Sources: EU EUDAMED, US FDA

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    MEICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSABLE AUTOMATIC BIOPSY INSTRUMENT

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

    MEDICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSALE SEMI-AUTOMATIC BIOPDY INSTRUMENT

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

    ACUSON Z6MS ULTRASOUND TRANSDUCER

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code ITX·January 3, 2018

    LIMA HIP

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code HXC·June 21, 2012

    DSX

    FDA Adverse Event
    DYNEX TECHNOLOGIES INC·Product code JQW·January 3, 2017

    LIMA HIP

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code LXH·June 21, 2012

    BIOPINCE

    FDA Adverse Event
    Malfunction ·MEDICAL DEVICE TECHNOLOGIES INC.·Product code KNW·January 18, 2008

    COBAS® 4800 BRAF V600 MUTATION TEST

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·May 24, 2024

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·February 20, 2026

    DE PUY ORTHO TECHNOLOGY

    FDA Adverse Event
    Other ·DEPUY ORTHOPAEDICS, INC.·Product code HTO·December 1, 1999

    COULTER® ACT 8/10 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·January 23, 2013

    ANGIOTECH

    FDA Adverse Event
    Malfunction ·MEDICAL DEVICE TECHNOLOGIES·Product code KNW·July 10, 2007

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·June 14, 2024

    2517506-2017-00415

    FDA Adverse Event
    Malfunction ·April 21, 2017

    PATH(R) THREAD CUP ADAPTOR, REF 2007-0013, Wright Medical Technology, Inc. Orthopaedic surgical instrument.

    FDA Enforcement
    Class II ·Terminated·Microport Orthopedics INC.·June 11, 2014

    ON-X CONFORM-X AORTIC PROSTHETIC HEART VALVE

    FDA Adverse Event
    Other ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·December 17, 2010

    SUREFORM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code GDW·December 18, 2024

    DIMENSION VISTA CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·July 29, 2014

    ENDOWRIST STAPLER 45 RELOAD

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL,INC.·Product code NAY·June 3, 2016

    ON-X PROSTHETIC MITRAL VALVE 27/29

    FDA Adverse Event
    Malfunction ·ON-X LIFE TECHNOLOGIES, INC·Product code LWQ·May 11, 2017