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

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    MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VARIAN V-3300, PHASED ARRAY ULTRASON

    FDA 510(k)
    FDA Class 2 ·Radiology

    MANDIBULAR LIP BUMPER AND LIP BUMPER TUBES

    FDA 510(k)
    FDA Class 1 ·Dental

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·March 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    ATTAIN ABILITY

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

    G7 NEUTRAL E1 LINER 36MM G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·September 23, 2020

    G7 PPS LTD ACET SHELL 58G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·September 23, 2020