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

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    UPSYLON Y MESH

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

    ArgenZ HT+ 95x25 A4

    FDA UDI
    ARGEN CORPORATION, THE·D818122794·Dental porcelain/ceramic restoration kit

    BD BBL¿ TRYPTICASE SOY AGAR WITH 5% SHEEP BLOOD (TSA II)

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·August 23, 2023

    BD ULTRA FINE PEN NEEDLES

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2020

    EOS SMALL BONE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E-SPEED EBT SCANNER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·August 8, 2022

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·May 21, 2013

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 3, 2011

    PRECISION XTRA/OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·August 13, 2008

    Ureteral dilator, REF RBD014

    FDA Enforcement
    Class II ·Ongoing·Coloplast Manufacturing US, LLC·April 10, 2024