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

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    STOPCOCK INTRAVENOUS THERAPY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRO

    FDA UDI
    Stryker GmbH·07613252714002·Basic Instruments Tray P&A System

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981195182·Interbody, 9mm x 40mm x 7mm, 0 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981203177·Interbody, 9mm x 40mm x 7mm, 0 deg

    ARTELON SPACER CMC-1

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LUXER SHADED ZIRCONIA

    FDA 510(k)
    FDA Class 2 ·Dental

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 26, 2012

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 18, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 28, 2015

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 30, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 6, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 28, 2015

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 1, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 12, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 5, 2016

    COMPRESS PROXIMAL TIBIAL SPINDLE

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code KRO·November 21, 2001

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·February 1, 2013

    COLLEAGUE CXE VOLUMETRIC INFUSION PUMP SINGLE CHANNEL RECERT

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 29, 2010

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X65 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·July 17, 2014

    COMPRESS ANCHOR PLUG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 13, 2018