BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    MODELS TA 1017 & 1017T GRITIFLO DISPOS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SKAFFOLD CIS

    FDA 510(k)
    FDA Unclassified ·Unknown

    ENDOPATH NON-BLADED SOLID OBTURATOR TROCAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TPRLC 133 MP TYPE1 PPS HO 15.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·June 5, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 15, 2014

    REVO MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWP·October 31, 2012

    ESPRIT VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·August 23, 2010