BEUDAMED
    25 results · 23ms · Sources: EU EUDAMED, US FDA

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    SYNTHES HIGH TIBIAL OSTEOTOMY (HTO) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INSTANTCHECK RTD-ECG MONITOR, MODEL RMH4.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AccuCath Intravascular Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·May 7, 2022

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·March 21, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 13, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 13, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 1, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 6, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·March 21, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·March 21, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 13, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·December 22, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·October 12, 2022

    SYMBIQ 3.13 DUAL CHA

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 11, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 15, 2013

    SUPER POLIGRIP AND POLIGRIP

    FDA Adverse Event
    Other ·GLAXOSMITHKLINE·Product code KOL·January 12, 2011

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 30, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 30, 2012

    IMMAGE® RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·January 6, 2012