BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    AERODR SYSTEM WITH P-31

    FDA 510(k)
    FDA Class 2 ·Radiology

    ZEUS-O

    FDA UDI
    SPINAL ELEMENTS·00840916122393·Zeus-O Implant, 13 x 9 x 36mm

    GYNECARE TVT ABBREVO CONTINENCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    RITA CLIPS FOR INFUSION PUMPS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 28, 2025

    GYNECARE TVT-ABBREVO MINI LCM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·November 30, 2021

    REFLEX-HYBRID SCREW EXTRACTOR

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-FRANCE·Product code LXH·January 8, 2015

    REFLEX-HYBRID SCREW EXTRACTOR

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-FRANCE·Product code LXH·January 8, 2015

    MONOPOLAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 24, 2013

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·September 30, 2014

    CARPENTIER-EDWARDS® PERIMOUNT® MAGNA MITRAL EASE¿ PERICARDIAL BIOPROSTHESES

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 16, 2011