BEUDAMED
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    DIGITAL FLAT PANEL X-RAY DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    Kitazato IUI Catheter

    FDA UDI
    KITAZATO CORPORATION·04580745041217·

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167521311140·

    CATHETER MOUNT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZO·October 24, 2014

    ADVANCIS ACTIVON TUBE

    FDA 510(k)
    FDA Unclassified ·Unknown

    PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523165476·L CR Tibial Insert Trial with Anterior Slot, Sz...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100965·L CR E-MAXTM Vitamin E Congruent Tibial Insert ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144457·L CR UHMWPE Congruent Tibial Insert Sz A 14mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101825·L CR MAXTM HXL Congruent Tibial Insert Sz A 14mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124046·L CR Tibial Insert Trial Sz A 14mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172344·CR Tibial Insert Trial with Posterior Pin Relie...

    SURESIGNS VS2+ NBP/SPO2/WIRELESS

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MHX·August 26, 2021

    Widex

    FDA UDI
    Widex A/S·05706069886320·WIDEX MOMENT MRB0 (Honey blond ) 330, RIC 10

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD/ HUNTINGTON·Product code HQL·May 23, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - BUFFALO GROVE·Product code FRN·June 16, 2011

    VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 6, 2014

    MICROPUNCTURE TRANSITIONLESS STIFFENED CANNULA ACCESS SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·April 4, 2018

    MICROPUNCTURE TRANSITIONLESS STIFFENED CANNULA ACCESS SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·November 15, 2017