BEUDAMED
    23 results · 23ms · Sources: EU EUDAMED, US FDA

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    SAFETY SUBCUTANEOUS TISSUE INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARGEDENT B YEL PF 5 dwt

    FDA UDI
    ARGEN CORPORATION, THE·D818120195·Gold based noble metal

    Diversatek Healthcare

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·M7831201950·Basic Endoscopy Procedure Kit

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319720196·Gruenwald Tissue Forceps 8" (20cm), 1x2 teeth, ...

    SIMIDUR S1S

    FDA 510(k)
    FDA Class 2 ·Dental

    NDS SURGICAL IMAGING, LLC FOR THE ZEROWIRE DUO WIRELESS HD VIDEO TRANSFER SYSTEM, MODEL WU-WX-WY (WHERE U=R OR T, W=P, X

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

    BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·May 13, 2022

    BD¿ NEEDLE 1 1/2 IN. SINGLE USE, STERILE, 18 G

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·February 24, 2022

    IN00087 CLERMONT FERRAND PH

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA·Product code DWF·March 7, 2014

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 14, 2015

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 15, 2015

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 13, 2014

    INSPIRE 6F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 7, 2016

    BD¿ NEEDLE 1 1/2 IN. SINGLE USE, STERILE, 18 G

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 24, 2022

    ULTRAFLEX? TRACHEOBRONCHIAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code JCT·May 20, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 25, 2014

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·June 6, 2011

    BD PRECISIONGLIDE NEEDLE 18G X 1 ½

    FDA Adverse Event
    Malfunction ·BD·Product code FMF·February 7, 2022

    INSPIRE 6F HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 21, 2022

    INSPIRE 6F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·June 8, 2016