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

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    Diode Laser Body Sculpture System

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

    HHM

    FDA UDI
    Oticon A/S·05707131351456·G500 SC, BTE PP 13 2.4G 105 C048 HHM

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001898·CODMAN SLIM-LINE Aneurysm Clip 45 Degree Angle ...

    ADAPT OPEN ACCESS PORT, MODEL 41233

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

    AVID-NIT LOSS OF RESISTANCE SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·January 10, 2019

    PDS PLATE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NHB·November 20, 2019

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code INM·October 27, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MTF·July 2, 2013

    COREVALVE REVALVING SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 2, 2017

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 6, 2017

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NIK·October 9, 2017

    PHYSIOMESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·May 6, 2019

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 10, 2018

    SELECTSECURE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·August 20, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·November 6, 2020

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·November 6, 2020

    FLEX 60 ARTICULATING

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 12, 2018

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 1, 2025