BEUDAMED
    7,036 results · 32ms · Sources: EU EUDAMED, US FDA

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    SOUTH WEST EXPOSURES (2566031 ONT INC.)

    FDA registration
    SOUTH WEST EXPOSURES (2566031 ONT INC.)·2 products·🇨🇦 Canada

    ALLEN

    FDA UDI
    HILL-ROM, INC.·00615521019761·Nissen Thigh Strap

    VINTAGE LD 15G ADD-ON T

    FDA UDI
    SHOFU DENTAL CORPORATION·E235L86620·VINTAGE LD 15G ADD-ON T

    Ohio

    FDA UDI
    OHIO MEDICAL, LLC·00628101608842·IFM 0-15LPM TUBE USA OXY OH TYPE T

    Ohio

    FDA UDI
    OHIO MEDICAL, LLC·00628101615987·IFM 0-15LPM TUBE USA OXY OH TYPE T

    Ohio

    FDA UDI
    OHIO MEDICAL, LLC·00628101616656·IFM 0-1LPM TUBE USA OXY OH TYPE T

    Ohio

    FDA UDI
    OHIO MEDICAL, LLC·00628101616236·IFM 0-15LPM TUBE US AIR OH TYPE T

    Ohio

    FDA UDI
    OHIO MEDICAL, LLC·00628101608590·IFM 0-15LPM TUBE US AIR OH TYPE T

    NGS-TurboPrep Library preparation for ONT(12)

    FDA UDI
    GenBio·00613745002347·

    NGS-TurboAmp Multiplex 11 loci for ONT (12)

    FDA UDI
    GenBio·00613745002323·

    ONTE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·December 27, 2005

    ONT TOUCH FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·December 20, 2005

    ONT TOUCH II

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·June 26, 2003

    ONT TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·July 15, 2005

    ONT TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·July 28, 2005

    ONT TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 2, 2002

    ONT TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·March 1, 2010

    ONT TOUCH ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·April 9, 2010

    ONT TOUCH ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·May 10, 2010

    ONT TOUCH BASIC ENCHANCED

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code CFR·June 19, 2001