BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    EXCEL PHOTIC STIMULATOR, MODEL (XLPS-1)

    FDA 510(k)
    FDA Class 2 ·Neurology

    BruxZir GT (Gum Tissue) Color

    FDA 510(k)
    FDA Class 2 ·Dental

    COULTER DIFF3 SYS. (COULTER #7400003)

    FDA 510(k)
    FDA Class 2 ·Hematology

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006

    MAMMOTOME HARDWARE HOLSTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code KNW·June 13, 2006

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 15, 2011

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014

    ACIST

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

    CORAIL2 STD SIZE 9

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWA·February 28, 2019