BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP

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

    Firebird Spinal Fixation System/Phoenix MIS Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDICINELODGE ZIPKNOT

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

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    PULSE-GENERATOR, PACEMAKER, EXTERNAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 6, 2011

    CORAIL2 STD SIZE 8

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS-3003895575·Product code KXA·July 22, 2014

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020