BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    PRONOSCO X-POSURE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984178·anteriors; shade A3.5; mould 101

    DRUG CONTROL SET

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    PATIENT EXAM GLOVES (MFG: GLOVES INT'L LTD.)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PORTEX® BIVONA® AIRE-CUF® NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JOH·March 28, 2017

    PORTEX®BIVONA® UNCUFFED NEONATAL AND PEDIATRIC TRACHEOSTOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD INC.,·Product code JOH·June 28, 2016

    CURRENT RF VR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·February 28, 2013

    ENDOPATH** XCEL* TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·February 10, 2011

    UNIVERSAL BOLT DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MAY·August 6, 2014