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

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    Steriking® LT-Blueline Pouches with Tyvek®

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ELEKTA LEKSELL STEREOTACTIC SYSTEM WITH MR POST KIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    HBA1C CONTROL, LEVEL 1 AND LEVEL 2

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·March 24, 1999

    ONE TOUCH BASIC

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code CFR·August 20, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·March 24, 1999

    HYDROVIEW INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·December 3, 2002

    HEARTSTART

    FDA Adverse Event
    Malfunction ·LAERDAL MEDICAL A/S·Product code MKJ·October 19, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO·Product code MGB·March 24, 1999

    PACESETTER

    FDA Adverse Event
    Injury ·OSCAR MEDICAL INC·Product code DTB·May 27, 1999

    9550 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·March 18, 1999

    V-CATH

    FDA Adverse Event
    Injury ·HDC CORP.·Product code DQO·December 27, 1999

    2183157-1999-00314

    FDA Adverse Event
    Malfunction ·December 23, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 11, 1999

    MEDTRONIC SYNCHROMED PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC INC./NEUROLOGICAL DIV.·Product code LKK·December 15, 1999

    M-ALGNT TUBE W/O RING

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code FZX·September 23, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 24, 1999

    9700 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·August 24, 1999

    MEDULLARY TUBE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code FZX·March 22, 1999

    EBI XFIX DYNAFIX

    FDA Adverse Event
    Injury ·ELECTRO-BIOLOGY, INC.·Product code HTY·September 15, 1999