BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100219·LIEBERMAN ASPIRATING SPECULUM K-WIRE

    GYMFORM DUAL FLEX BELT MODEL WB-162

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GRAFTCAGE TLX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLEARVIEW UTERINE MANIPULATOR

    FDA Adverse Event
    Injury ·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024

    ATTAIN ABILITY MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·June 7, 2013

    COLLEAGUE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 6, 2011

    ACTIVA

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code MHY·October 8, 2014

    STAPLE NITINOL 10 X 10 FUSEFORCE

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY INC·Product code JDR·August 19, 2022