BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Advance Biliary Balloon Catheter

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

    Neuro Cochlear Implant System

    FDA UDI
    NEURELEC·03663227004007·Programming Device, Right Wired

    Accent 1400 TouchGuide 4 Location

    FDA UDI
    PRENTKE ROMICH COMPANY·00858526006118·TouchGuides are made from clear polycarbonate m...

    SPECBOARD JR.

    FDA 510(k)
    FDA Class 2 ·Radiology

    VENUS CERVICAL SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø32/+0MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 5, 2019

    RECAP FEM HD COCR CEMENTED DIA50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 15, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 17, 2013

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code MMH·July 23, 2011

    REVERSE SHOULDER SYSTEM GLENOID BASEPLATE Ø22X15

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·May 19, 2020