BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    MYLABSSOGNO

    FDA 510(k)
    FDA Class 2 ·Radiology

    ForPro

    FDA UDI
    Tng Worldwide, Inc.·00672047101592·White Nitrile Glove Size Large 100ct

    COMBI SELF PROPELLED SHOWER COMMODE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    LYMPHA PRESS 201MAX, MODEL 201MAX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·May 31, 2013

    ELECTRIC STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·June 15, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·September 3, 2008

    Retractor f/Sciatic Nerve; Part number: 03.100.013; UDI: 10886982070623

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·May 16, 2018

    Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator

    FDA Enforcement
    Class II ·Ongoing·Boston Scientific Corporation·September 25, 2019