BEUDAMED
    188 results · 29ms · Sources: EU EUDAMED, US FDA

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    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·GUARDIAN(R) ATP II IMPLANTABLE CARDIOVERTER/DIFIB.

    VARIAX

    FDA UDI
    Stryker GmbH·07613327005882·Clav Tray 2 Level

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295223481·SIGMA FEMORAL CRUCIATE RETAINING POROCOAT SIZE ...

    MANAN GENERAL PURPOSE INTRODUCER NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Gibralt Spine System

    FDA UDI
    Choice Spine, LP·00840996169844·GIBRALT,DRILL,ADUSTABLE,2.4

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

    PORTEX CO2 CLIP

    FDA Adverse Event
    Death ·SMITHS MEDICAL ASD, INC.·Product code CCK·November 9, 2005

    NUCLEUS 22

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code MCM·May 18, 2025

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·April 13, 2012

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·May 16, 2008

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·March 29, 2007

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·April 14, 2011

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·November 26, 2008

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LNM·March 29, 2007

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·February 1, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 28, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2014

    Stimulator, Hypoglossal Nerve, Implanted, Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·Genio® System 2.1

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·RESTYLANE INJECTABLE GEL

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LNM·April 20, 2007