BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    AIRLIFE BUBBLE HUMIDIFER, MODEL 002003 AND 002006

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NOVABONE DENTAL PUTTY - BIOACTIVE SYNTHETIC BONE GRAFT

    FDA 510(k)
    FDA Class 2 ·Dental

    Renuvion/J-Plasma Precise Handpiece

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

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 6, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·January 28, 2011

    CAPSUREEPI

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