BEUDAMED
    1,298 results · 22ms · Sources: EU EUDAMED, US FDA

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    ELECTRONIC MUSCLE STIMULATOR - MICROSTIM J-1304D

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CLYDESDALE PTC™ Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169190368·CAGE 4980040 CDALE PTC 18MM 0 DEG 10X40

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980040·DeltaForm HD upper posteriors, XL, A4 -MADE IN ...

    Gibralt Spine System

    FDA UDI
    Choice Spine, LP·00840996169875·GIBRALT,TAP,NO SLEEVE,4.0

    NC TREK™ RX Coronary Dilatation Catheter; NC TREK™ OTW Coronary Dilatation Catheter; TREK™ RX Coronary Dilatation Catheter; TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ RX Coronary Dilatation Catheter; MINI TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ II OTW Coronary Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ORTHO ALL-FLEX DIAPHRAGM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    TECNIS 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·January 6, 2014

    TECNIS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·November 20, 2015

    MULTIFOCAL IOLS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·April 1, 2019

    TECNIS 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code MFK·April 26, 2019

    TECNIS

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code MFK·March 29, 2018

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code POE·March 23, 2021

    TECNIS SYMFONY

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·March 23, 2018

    TECNIS SYMFONY TORIC

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·September 11, 2019

    LIBERTY CYCLER

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·June 25, 2014

    EXCLAIM 8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 22, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 24, 2011

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·SENSAR SOFT ACRYLIC UV-LIGHT ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS

    TECNIS ODYSSEY TORIC II IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·April 28, 2025

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·October 24, 2023