BEUDAMED
    27 results · 27ms · Sources: EU EUDAMED, US FDA

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    AYON Body Contouring System (AYON SYSTEM)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517199119·MaXcess 4 Aluminum Blade, 50mm Ctr

    Breast Localization Needles

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333003747·Hawkins™ III Hardwire BLN with Echogenic Tip 20...

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690125150·Femoral Augment Posterior, Size 4+, 5mm

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690126584·Femoral Posterior Augment Trial Size 4+, 5mm

    HALYARD® ONE-STEP® Sterilization Wrap, HALYARD® QUICK CHECK® Sterilization Wrap, HALYARD® SEQUENTIAL Sterilization Wrap and HALYARD® SMART-FOLD® Sterilization Wrap

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENT Nasopharyngoscope and Accessories

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    IMPL TAPERED SCR-V MTX 3.7MM 3.5MM 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·October 24, 2022

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·August 24, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2013

    M2A MAGNUM MODULAR HEAD 46MM HEAD DIAMETER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 31, 2016

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 3, 2018

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 3, 2018

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 22, 2017

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2018

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 6, 2018

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 12, 2018

    BD DISCARDIT II¿ SYRINGE WITH NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 28, 2018

    M2A-MAGNUM MOD HD SZ 46MM

    FDA Adverse Event
    Injury ·.·Product code KWA·June 8, 2017