BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    TRACHEAL TUBE FIXATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MP VIAL ADAPTER 13MM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDISISS PHACOEMULSIFICATION TIPS/NEEDLES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    INSERTER/EXTRACTOR FOR CHILD & ADOLESCENT OSTEOTOMY PLATES

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWB·March 26, 2020

    LIGACLIP** ENDOSCOPIC

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·December 16, 2010

    10MM TI CANNULATED TIBIAL NAIL-EX/330MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code JDS·January 25, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 11, 2014

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 29, 2019

    EVOLUT PRO TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 29, 2019

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 5, 2015

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 9, 2015

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 30, 2018