BEUDAMED
    6,886 results · 32ms · Sources: EU EUDAMED, US FDA

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    SFTWR MMT-8061 INPEN APP ANDROID

    FDA Adverse Event
    Malfunction ·COMPANION MEDICAL INC·Product code NDC·May 14, 2024

    DAVINCI SI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·December 2, 2024

    SPECIALTY JDK TENSIONING

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·March 2, 2015

    Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling: JADAK JDK-2330 REV B 170512-017

    FDA Recall
    Terminated ·Luminex Corporation·Product code OOI·June 29, 2018

    Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling: JADAK JDK-2330 REV B 170512-017

    FDA Enforcement
    Class II ·Terminated·Luminex Corporation·August 28, 2019

    SECUR-FIT HA PSL CUP/CLUSTR SHELL 52MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDK·August 13, 2015

    ALLEN MEDULLARY CEMENT PLUGS

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JDK·May 14, 2010

    CEM RESTRICTOR LG

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDK·May 14, 2010

    HYDROSORB CR 8X 22 MM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK - MEMPHIS·Product code JDK·January 2, 2004

    CEMENTRALIZER 10.0MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDK·April 15, 2021

    CEMVAC 1 PIECE GUN

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 3015516266·Product code JDK·May 18, 2022

    UNKNOWN OMNIFLEX STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDK·February 24, 2012

    SECUR-FIT HA PSL CUP/CLUSTR SHELL 52MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDK·August 14, 2015

    BIOPREP

    FDA Adverse Event
    Malfunction ·STRYKER CORPORATION·Product code JDK·June 11, 2021

    UNIDENTIFIED ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code JDK·August 24, 2015

    RV. UNIVERSAL CEMENT RESTRICTOR

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDK·November 24, 2008

    BIO-PREP BONE PREPARATION KIT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code JDK·March 28, 2013

    SECUR-FIT HA PSL CUP/CLUSTR SHELL 52MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDK·February 15, 2013

    BIO-PREP BONE PREPARATION KIT

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS PUERTO RICO·Product code JDK·October 19, 2009

    BIOPLEX IMPLANT

    FDA Adverse Event
    Other ·INTERPORE CROSS INTERNATIONAL·Product code JDK·June 28, 2005