BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    AS3000 OPERATIVE DENTAL UNIT (DELIVERY SYSTEM)

    FDA 510(k)
    FDA Class 1 ·Dental

    Couture Essence

    FDA UDI
    Carolon Company·00078301931248·

    DENTAPORT ZX

    FDA 510(k)
    FDA Class 1 ·Dental

    ADVANCE CS CORONARY SINUS INFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·March 8, 2026

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·January 15, 2024

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code PFO·January 15, 2024

    ACRYSOF

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD.·Product code HQL·June 10, 2014

    NCB-PH TORQUE WRENCH 4 NM

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code HXC·January 22, 2013

    PUMP MMT-722NAL PRDGM INSULIN CL EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·December 10, 2010

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·February 3, 2017

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·March 10, 2017

    ELECSYS ESTRADIOL III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CHP·May 4, 2026