BEUDAMED
    9 results · 30ms · Sources: EU EUDAMED, US FDA

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    RABEA DEVICE, MODEL PXXXXXX

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

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377080776·RELINE C Tap, Ø4.5mm Extended

    417 P37,GE,1L,2LD,STD,STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828100342·417 P37,GE,1L,2LD,STD,STKR

    VPC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MENDASIL TWG GEL ANTIMICROBIAL SKIN AND WOUND GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    APPLICAT OUT SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·March 5, 2013

    NC QUANTUM APEX PTCA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·February 15, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 7, 2014

    EMBRYO RPLCMNT CATHETER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019