BEUDAMED
    8 results · 27ms · 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 ×

    QBC STAR CENTRIFUGAL HEMATOLOGY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    BLOOD COLLECTION TUBE SAMPLES FOR USE WITH POINT OF CARE BLOOD ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    UNICATH A

    FDA 510(k)
    FDA Class 2 ·Radiology

    EARIGATOR

    FDA Adverse Event
    Malfunction ·SURYA TECHNOLOGIES INTERNATIONAL·Product code JYH·January 4, 2001

    NOTINGHM SHLDR HUM HEAD 48X17 OFFSET

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·January 19, 2016

    9.0MM FLEXIBLE MEDULLARY REAMER/FLAT WIRE/385MM

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·March 7, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 4, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code NVZ·August 8, 2014