BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Estremo Citieffe Nailing System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Disect Gen Surg

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101049·WRIGHT FASCIA NEEDLE

    INFINION 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 18, 2023

    ZEGRA POSTURE TRAINER

    FDA 510(k)
    FDA Unclassified ·Unknown

    GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE

    FDA 510(k)
    FDA Class 2 ·Dental

    3.5MM LCP SUPERIOR CLAVICLE PLATE/7 HOLE/RIGHT/100MM

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·August 15, 2017

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·June 21, 2013

    CP85341 FR PARIS

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 25, 2008

    DURASUL LINERS

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·May 7, 2024