BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    REFLECTION DUAL DIMENSION SHELL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556863992·RSS HUMERAL BODY INSERTER/ EXTRACTOR KNOB

    SPONGE, CURITY WASHED GAUZE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TitanTM

    FDA UDI
    Ascension Orthopedics, Inc.·10381780527022·Reverse Shoulder System Humeral Body Inserter/E...

    HUMERAL BODY INSERTER/ EXTRACTOR KNOB

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code LXH·June 29, 2017

    HUMERAL BODY INSERTER/ EXTRACTOR KNOB

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code LXH·June 29, 2017

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 29, 2014

    LITHOTOMY PACK IV

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK HEALTH CARE·Product code KKX·February 13, 2013

    SD/PD LONG CURVED

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·December 17, 2010

    HUMERAL BODY INSERTER/ EXTRACTOR KNOB

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code LXH·July 7, 2017