BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)

    FDA 510(k)
    FDA Class 2 ·Neurology

    FPS

    FDA UDI
    Tyber Medical, LLC·00810040686207·Ø2.5mm Non-locking Screw, 34mm

    ceraMotion®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011251034200·ceraMotion® Ti Base Dentin D2, 20 g / dental ce...

    ceraMotion®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011251034400·ceraMotion® Ti Base Dentin D2, 40 g / dental ce...

    PainKARE

    FDA 510(k)
    FDA Class 2 ·Neurology

    URYXXON 200 URINE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NA

    FDA UDI
    aap Implantate AG·04042409194474·Cortical Screw 2.5, self-tapping, L 34

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PML·February 26, 2026

    EXTENSION SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·November 14, 2014

    QUICKSET 3.8 DIMTR DR BIT 25MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·August 26, 2011

    HEARTMATE II LVAD

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·July 23, 2013

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PML·November 13, 2025