BEUDAMED
    9 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 ×

    A-JUST TURBIDITY METER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283136·DEAVER RETRACTOR HOLLOW 1" X 13"

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209109944·KIT, SRO CRISIS RESPONSE - ORG

    R350 guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EnSite™ X EP System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    I-STAT1 ANALYZER, IMMUNO READY, WIRELESS

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CGA·January 26, 2021

    DEPUY ASR XL FEM IMP SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 29, 2012

    COBAS AMPLIPREP / COBAS TAQMAN ANALYZER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNSOTICS, LTD.·Product code JJF·October 4, 2010

    CARE ASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·March 25, 2014