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

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    Sapphire NC Plus

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JOSEPH PERIOSTEAL ELEVATOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896018327·JOSEPH PERIOSTEAL ELEVATOR CURVED TIP

    K162309

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code PGW·November 14, 2019

    BASX BLADELESS TROCAR

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

    ENCODE PATIENT SPECIFIC ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 6, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 3, 2013

    IX FEMUR MESH PA MIDI 300 L

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·July 7, 2011

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 16, 2008

    Exactech Equinoxe REVERSE SHOULDER,42mm Constrained Humeral Liner, a) +0mm, Item number 320-42-10, b) +2.5mm, Item Number 320-42-13; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024