BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    HARD TISSUE REPLACE(HTR(R))-PATIENT-MATCH IMPLANT

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

    Burr

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113165·DIAMOND BURR 5.0MM DIAMETER DISC

    HEART PACK II

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

    RESPIRONICS' DIGITAL MANOMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD BBL¿ TAXO¿ DIFFERENTIATION DISCS FOR V FACTOR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTO·January 19, 2023

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 22, 2013

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·December 10, 2010

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 10, 2014

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024