BEUDAMED
    7 results · 17ms · 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.

    KAVOKLAVE STEAM AUTOCLAVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756566186·DRP BRACH ANGIO 44X31 W/3``

    SYNTHES STERNAL ZIPFIX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CANNULA, SURGICAL GENERAL & PLASTIC SURGERY, MODELR65-995, R65-995-1, R65-995-2, R65-997, R65-997-1

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

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FRN·January 8, 2013

    AGILIS NXT KIT, 71CM, MEDIUM CURL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIV·Product code DYB·November 23, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 2, 2014