BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    BIOSTINGER-V BIOABSORBABLE MENISCAL REPAIR DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCOLITH 2000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Endoscope Tip Protector - Sterile, Endoscope Tip Protector - Non-sterile

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 6, 2013

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·August 8, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 30, 2024

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 30, 2024