BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MEDLINE PROHIBIT SERIES SURGICAL MASK WITH FLUID SHIELD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MARKSMANN CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    UNKNOWN MICROCATHETER

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code DQY·May 30, 2017

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·March 6, 2013

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014