BEUDAMED
    16 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.

    HEMOCUE PHOTOMETER TECHNICAL MANUAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    NOVEOS Diluent A Kit

    FDA UDI
    HYCOR BIOMEDICAL LLC·00816879028829·

    NOVEOS Diluent A Kit

    FDA UDI
    HYCOR BIOMEDICAL LLC·00816879029628·

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153936·

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153929·

    51CM(20.1INCH) TFT MONOCHROME LCD MONITOR, MU5111BW

    FDA 510(k)
    FDA Class 2 ·Radiology

    ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCUTORR PLUS MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·March 7, 2014

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·November 14, 2012

    CONSTELLATION WITH LASER

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 3, 2010

    ACCUTRAK DELIVERY CATHETER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 20, 2019

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 20, 2019

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 20, 2019

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 4, 2022

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·September 20, 2023

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·September 19, 2022