BEUDAMED
    402 results · 26ms · Sources: EU EUDAMED, US FDA

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    HILGER DUAL-STIM NERVE STIMULATOR

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

    Gibralt

    FDA UDI
    Choice Spine, LP·10885862145239·

    Gibralt®

    FDA UDI
    INNO Holdings, Inc.·M711050040635600·Posterior Cervical Combination Connector, 3.5-6...

    MAR COR SERVICES BICARB SYSTEM

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

    SEMPERMED SUPREME, SIZES 5.5, 6, 6.5, 7, 7.5, 8, 8.5, AND 9

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

    EQUINOXE REVERSE 38MM HUMERAL LINER +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 17, 2022

    TI-DBLE LEAD CORT SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSB·August 24, 2018

    ENTRAK 2500

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·April 12, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·April 19, 2011

    OXIMAX N-595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·COVIDIEN FORMERLY TYCO HEALTHCARE·Product code DQA·June 18, 2008

    EQUINOXE REVERSE 46MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 2, 2024

    EQUINOXE REVERSE 42MM HUMERAL LINER +2.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 4, 2023

    EQUINOXE REVERSE TRAY ADAPTER PLATE TRAY +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 11, 2024

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 20, 2020

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026