BEUDAMED
    34 results · 26ms · Sources: EU EUDAMED, US FDA

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    Artemis Proximal Femoral Nail System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    24M - Tampa Electric Co.

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.

    36M - Navajo Tribal Utility Authority

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588012797·36M - Navajo Tribal Utility Authority

    SCS CLARIS SPINAL SYSTEM, LENGTHENED LATERAL CONNECTOR, MODEL AL06

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Super Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACUTRAK MINI

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HWC·January 24, 2019

    ACUTRAK MINI

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HWC·January 24, 2019

    ACUTRAK MINI

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 24, 2019

    ACUTRAK MINI

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HWC·January 24, 2019

    ACUTRAK MINI

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HWC·January 24, 2019

    GORE PROPATEN VASCULAR GRAFT

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code DSY·October 17, 2008

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·June 27, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 3, 2011

    UNKNOWN TIBIAL SPACER COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·October 2, 2017

    UNKNOWN FEMORAL SPACER COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·October 2, 2017

    UNKNOWN STAGEONE KNEE CEMENT SPACER MOLD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 29, 2017

    UNKNOWN STAGEONE KNEE CEMENT SPACER MOLD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 29, 2017

    BIOMET STAGE ONE CEMENTED FEMORAL MOLD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·October 2, 2017

    UNKNOWN FEMORAL SPACER COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 2, 2017

    BIOMET STAGE ONE CEMENTED TIBIAL MOLD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·October 2, 2017