BEUDAMED
    9 results · 21ms · 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.

    SPACELABS MODEL 90900

    FDA 510(k)

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150690·K-WIRE - SINGLE TROCAR 0.9mm DIA x 75mm

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978075815·INSTRUMENT 894 093 GUIDE WIRE DIA O.093

    JCM LABS CUSTOM PRESCRIPTION & ACCENT IN-THE-EAR

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    PERFORATOR BUR

    FDA 510(k)

    DR. SCHOLL'S CUSTOM FIT ORTHOTICS

    FDA Adverse Event
    SCHERING-PLOUGH CORP·Product code KNP·March 9, 2012

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 25, 2014

    WALLSTENT ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·November 9, 2010

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020