BEUDAMED
    20 results · 24ms · Sources: EU EUDAMED, US FDA

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    RANAWAT/BURSTEIN POROUS TOTAL HIP FEMORAL COMP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909116852·REVELATION DIAMOND 368-023SC - 5 PACK

    IP TEMP CEMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    BISTITE II DC

    FDA 510(k)
    FDA Class 2 ·Dental

    COBALT CHROME FEMORAL HEAD SZ 28 3.5MM 12/14 SHORT NECK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JDI·December 15, 2016

    COCR HEAD SHORT NECK DIA28/-3. 5 MM 12/14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDI·May 10, 2016

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    BIOMET COBALT-CHROME FEMORAL COMPONENTS

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·March 17, 2017

    COBALT CHROME FEMORAL HEAD

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code JDI·August 31, 2017

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 28, 2014

    CERTAS INLINE VLV ONLY

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·January 11, 2013

    PINN CAN BONE SCREW 6.5MMX15MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code NDJ·November 29, 2010

    BIOMET COBALT-CHROME FEMORAL COMPONENTS

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

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-N334 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 10, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018