BEUDAMED
    11 results · 31ms · Sources: EU EUDAMED, US FDA

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    VENTRICULAR LEAD, MODEL 6959

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517360465·CoRoent SI Rasp, 7x17x14mm

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515204218·Narrow Nose Wire Pulling Fcps, 7 1/2"

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790143000·discovery® Bracket with hook, - 17° Torque, 0° ...

    LARS AC Band Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SERUM, ALPHA-1-GLYCOPROTEIN ANTI-HUMAN

    FDA 510(k)
    FDA Class 1 ·Immunology

    STYLE 115 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·March 18, 2024

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·May 5, 2014

    DA+ C SERIES DR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DXY·October 15, 2012

    ZENITH RENU AAA ANCILLARY GRAFT MAIN BODY EXTENSION

    FDA Adverse Event
    Injury ·COOK INC·Product code MIH·August 3, 2010

    DIALYZER

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·September 23, 2024