BEUDAMED
    41 results · 23ms · Sources: EU EUDAMED, US FDA

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    GENIUS 2 INFRARED TYMPANIC ELECTRONIC THERMOMETER, MODEL 303000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70606491·Sprint II Bracket Roth .018" 400 Brackets 3-5 w...

    SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-1500

    FDA 510(k)
    FDA Class 2 ·Hematology

    EXHALE DOPPLER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TESS HUM INSERT TH 6 DIA36 S1

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·March 7, 2017

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    TESS HUMERAL REVERSED INLAY 036 S1 12MM

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 9, 2017

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    CUSTOM REVERSE HUMERAL LINER

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 27, 2017

    TESS GLEN BASEPLATE S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 25, 2016

    TESS HUMERAL REVERSE COROLLA S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·November 18, 2016

    UNKNOWN TESS GLENOID COMPONENT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·July 7, 2017

    TESS HUM INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 10, 2017

    UNKNOWN TESS HUMERAL INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·June 1, 2017

    NUVASIVE LATERAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code KWQ·March 26, 2013

    SENSOR ENLITE MMT-7008A

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZO·September 4, 2014

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·April 18, 2011

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 17, 2017

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·January 25, 2017

    TESS HUM INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 6, 2017