BEUDAMED
    17 results · 26ms · Sources: EU EUDAMED, US FDA

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    Splashwire Hydrophilic Guide Wire (MSWSTD35180J1O5); Splashwire Hydrophilic Guide Wire (MSWSTD35260J1O5); Splashwire Hydrophilic Guide Wire (MSWSTDA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35260LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFS38150LT)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EnSite Velocity Cardiac Mapping System, EnSite Precision Cardiac Mapping System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CUSTOM-HIP TOOL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD BBL¿ SALMONELLA SHIGELLA AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·January 17, 2023

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·December 16, 2014

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·December 16, 2014

    BD BBL¿ SALMONELLA SHIGELLA AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·February 24, 2023

    Titan T 5K Motor Product Usage: Low-speed motor is used with various attachments to perform a variety of dental procedures including caries removal, finishing, polishing, pin setting and prophy.The motor has a speed range of 100 to 5000 rpm capability.

    FDA Recall
    Terminated ·Dental EZ Group Star Dental Division·Product code EFA·June 13, 2014

    Titan T 5K Motor Product Usage: Low-speed motor is used with various attachments to perform a variety of dental procedures including caries removal, finishing, polishing, pin setting and prophy.The motor has a speed range of 100 to 5000 rpm capability.

    FDA Enforcement
    Class II ·Terminated·Dental EZ Group Star Dental Division·July 23, 2014

    BD BBL¿ SALMONELLA SHIGELLA AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·March 15, 2023

    BD BBL¿ SALMONELLA SHIGELLA AGAR PLATE 20PK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·March 7, 2023

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·December 16, 2014

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 5, 2014

    LIFEPAK 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·August 10, 2011

    UNICEL® DXC 800 SYNCHRON® SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·July 29, 2013

    BD BBL¿ SALMONELLA SHIGELLA AGAR PLATE 20PK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSI·March 14, 2023

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014