BEUDAMED
    192 results · 33ms · Sources: EU EUDAMED, US FDA

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    BONE BLOCK FIXATION SET

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526827936·ACHIMED ACHILLES SUPP BLACK V

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00505151·

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526827875·***DISC*LEVAMED ANKLE SUPPORT BLACK V

    MODIFICATION TO SYNERGY SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code MMI·June 18, 2012

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·May 10, 2006

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code MMI·June 14, 2012

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code MMI·June 15, 2012

    TRIAGE CARDIAC PANEL TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·June 27, 2012

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code MMI·June 14, 2012

    TRIAGE CARDIAC PANEL TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·June 27, 2012

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code MMI·June 18, 2012

    TRIAGE CARDIAC PANEL TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·June 21, 2012

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code MMI·July 5, 2012

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code GIS·February 6, 2006

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code GIS·February 6, 2006

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS(SLC)·Product code JAA·April 8, 2013

    AFFIRMITY DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008