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

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    UST-5268P-5 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930795060710·Fukashima Suction Tube 160mm 7 fr

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867141278·UNIVERS APEX HUM BROACH ALIGNMNT GD

    SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (HAND & NEURO)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Osseoflex SB Straight Balloon, 10g/4ml, Osseoflex SB Straight Balloon, 10g/2ml

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APPLIANCE, FIXATION DEVICE, PROXIMAL FEMUR

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDO·November 13, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2014

    HEARTMATE II LVAD

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·February 5, 2013

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·December 29, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. HUNTINGTON·Product code HQL·July 11, 2014