BEUDAMED
    11 results · 19ms · 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.

    TurboSEAL Nasogastric Aspiration Tube

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

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613021696·Ferguson Frazier Suction Tube, Angled, 9 French...

    INVACARE PRO, COMPACT AND PORTABLE DESKTOP

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SUNSET HEALTHCARE SOLUTIONS BACTERIAL/VIRAL HME FILTER, MODEL BHF 104

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 29, 2019

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 18, 2015

    CONNECSCR F/UTN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 3, 2013

    KNEE IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. ORTHOPAEDIC DIVISION·Product code JWH·June 28, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Injury ·ANGIOSCORE, INC·Product code LIT·March 29, 2016

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 26, 2015