BEUDAMED
    8 results · 19ms · 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.

    SOFTINJECT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    11G BLADED MAMMOTOME ST PROBE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006

    DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AZUR Vascular Plug

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AZUR VASCULAR PLUG 8

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code KRD·March 29, 2022

    CONSERVE(R) SUPER FINISH FEMORAL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KXA·March 6, 2013

    ADAPTA DR

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

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014