BEUDAMED
    20 results · 21ms · Sources: EU EUDAMED, US FDA

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    SCISSORS, IRIS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813056189·WIRE NI-TEK RD PREFORM /L .018 PK10

    Washbon

    FDA UDI
    ORMCO CORPORATION·00889989043488·UPPER RIGHT FIRST MOLAR WASHBON BAND SIZE 19

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700191·Mand. 2. Bicuspidband right 19

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190127·TIBIAL ANTERIOR SPIKE ASSY

    Navigational Instruments

    FDA UDI
    Seaspine Orthopedics Corporation·10889981148393·Navigation Sierra Screwdriver

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700190101·Mand. 2. Bicuspidband right 19

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700190051·Mand. 2. Bicuspidband right 19

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700190501·Mand. 2. Bicuspidband right 19

    INRATIO2 PT/INR PROFESSIONAL TEST STRIP

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·September 9, 2015

    INRATIO2 PT/INR TEST STRIP

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·March 4, 2016

    Aquilion Lightning, TSX-036A/1, V8.4

    FDA 510(k)
    FDA Class 2 ·Radiology

    CARRARA VOLUMIA

    FDA 510(k)
    FDA Class 2 ·Dental

    INRATIO2 PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·August 19, 2015

    INRATIO2 PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·May 4, 2016

    INRATIO2 PT/INR TEST STRIP

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·March 31, 2016

    INRATIO2 PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·December 15, 2015

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 28, 2014

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 3, 2012

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC IRELAND LTD.·Product code MAF·July 25, 2010