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

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    Artemis Diode Laser System (RL-S20S-TWC, RL-S20S-810B, RL-S20S-755)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IdentiTi

    FDA UDI
    ALPHATEC SPINE, INC.·00190376372648·DENTITi ALIF SA, T40 Driver, Angled, 40°, Short

    IdentiTi

    FDA UDI
    ALPHATEC SPINE, INC.·00190376372655·DENTITi ALIF SA, T40 Driver, Angled, 60°, Short

    VOLAR RADIUS PLATE WITH ANGULAR STABILITY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Disposable Surgical Mask

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 27, 2023

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·November 6, 2014

    UNICEL® DXC 800 SYNCHRON® SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 3, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 18, 2013

    OMNIPOD DASH INSULIN MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·January 7, 2025

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 8, 2018

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 8, 2018