BEUDAMED
    25 results · 29ms · Sources: EU EUDAMED, US FDA

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    AssureTech Secobarbital Strip, AssureTech Oxycodone Strip, AssureTech Secobarbital/Oxycodone Panel Dip, AssureTech Secobarbital/Oxycodone Quick Cup, AssureTech Secobarbital/Oxycodone Turn Key-Split Cup

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ProLift Expandable Spacer System

    FDA UDI
    Life Spine, Inc.·00190837065775·

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290314·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290437·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290284·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575290369·Orthopaedic implant aiming/guiding block, reusa...

    QMS ZONISAMIDE REAGENTS, CALIBRATORS AND CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CELL-DYN 22 PLUS CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008102·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008126·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008157·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008140·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008133·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008119·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·December 13, 2016

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·June 30, 2011

    DAMON COPPER NITI WIRE

    FDA Adverse Event
    Malfunction ·ORMCO CORPORATION·Product code DZC·September 9, 2008

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 6, 2016

    PROTEGE RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·COVIDIEN·Product code NIM·June 23, 2016