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

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    Filters Regulation: Us FDA ×

    SurgTech Thoracolumbosacral (TLS) Posterior Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221046178·Unitek(TM) Molar Band General Purpose Wide Hard...

    ZEUS ELISA HSV GC-I IGG TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SROM STM STD 36+12L 13X18

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code MRA·July 8, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 9, 2008

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 10, 2024

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·September 7, 2022