BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    “POINT” Kinguide Agile Hybrid Navigation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    EVONOS

    FDA UDI
    Gyrus ACMI, LLC·00821925019515·EAR SUCTION NEEDLE 22 GA

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180160286·Reversible Retractor (Left/Right)

    RM52260041 DS10014122 BI MENTUM RK PE LINER 22 41

    FDA Adverse Event
    Injury ·S.E.R.F SOCIETE DETUDES RECHERCHE FABRICATION·Product code MEH·January 24, 2025

    PANPAC WORD/BARTHOLIN CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DXTEND GLENOSPHERE STD D42MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS 3003895575·Product code KWS·June 25, 2015

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·November 17, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 31, 2011

    LOCKING HOLDING SLEEVE- STANDARD FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·July 16, 2013

    BACFIX ROD, UNKNOWN

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code HSB·January 16, 2020