BEUDAMED
    12 results · 20ms · 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 ×

    Instru-Safe Instrument Protection System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAT PLATFORM,HYDR/ELEC,GRAY,6X8',20-30"

    FDA UDI
    Hausmann Enterprises, LLC·00840314800992·

    MAT PLATFORM,HYDR/ELEC,BLACK,6X8',20-30"

    FDA UDI
    Hausmann Enterprises, LLC·00840314801012·

    MAT PLATFORM,HYDR/ELEC,BLUE,6X8',20-30"

    FDA UDI
    Hausmann Enterprises, LLC·00840314800985·

    MAT PLATFORM,HYDR/ELEC,GREEN,6X8',20-30"

    FDA UDI
    Hausmann Enterprises, LLC·00840314801005·

    MEDICOMPASS CONNECT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SECRMARK BIOPSY SITE MARKING SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD¿10ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMF·September 22, 2023

    NOBLUS ULTRASOUND SCANNER

    FDA Adverse Event
    Malfunction ·Product code IYO·March 30, 2017

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·May 24, 2013

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·June 20, 2011

    MODEL NOT SPECIFIED

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·August 27, 2008