BEUDAMED
    34 results · 22ms · Sources: EU EUDAMED, US FDA

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    ACE STAPLER AND CARTRIDGE

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

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306818813·Abdominal Wall Retractor, 2in x 10in

    POWDER FREE ELASTIC VINYL EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    EASYRA SODIUM ASSAY, EASYRA POTASSIUM ASSAY, EASYRA CHLORIDE ASSAY, EASYRA CARBON DIOXIDE ASSAY MODEL CAT NO. 5423 & 520

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    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

    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:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 18, 2016

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·November 2, 2012

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·July 22, 2015

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 15, 2012

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·February 27, 2015

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·December 23, 2013

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 9, 2013

    LIBERTY CYCLER

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·September 10, 2014

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 1, 2011