BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123199·K-WIRE - SINGLE TROCAR THREADED 2.0mm DIA x 150mm

    PUNZON CHEMOCLAVE PARA BOLSA/BOTELLA CON FILTRO DE VENTEO

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code ONB·February 8, 2021

    IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Fujifilm Ultrasonic Processors SU-1 PLATINUM and SU-1

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

    CAPSURE SP 4024

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    FORTIFY DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 23, 2014

    KIMVENT* MICROCUFF* ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK HEALTH CARE·Product code BTR·January 7, 2011

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026