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

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    LYSOL I.C. BRAND INSTRUMENT DISINFECTANT PRESOAK

    FDA 510(k)
    FDA Class 1 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122956·K-WIRE - SINGLE TROCAR 0.8mm DIA x 75mm

    ALLOX2 TISSUE EXPANDERS

    FDA 510(k)
    FDA Unclassified ·Unknown

    TRIFLANGE II ACETABULAR CUP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HL20 BUBBLE SENSOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015

    UNKNOWN NEXGEN LPS-FLEX COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 18, 2014

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·February 2, 2013

    AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB, INC.·Product code HQL·December 20, 2010

    3.0 RIO® ROBOTIC ARM - MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 14, 2018

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020