BEUDAMED
    1,127 results · 16ms · Sources: EU EUDAMED, US FDA

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    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·March 30, 2023

    KNE-UNK-LPS FLEX TIBIA OPTION SIZE 4

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 30, 2023

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·May 29, 2026

    Ultradent Products, Inc. Paper Points, Size 25 PN #1554, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code EKN·August 4, 2017

    Ultradent Products, Inc. Paper Points, Size 45 PN #1558, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins..

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code EKN·August 4, 2017

    Ultradent Products, Inc. Paper Points, Size 30 PN #1555, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code EKN·August 4, 2017

    Ultradent Products, Inc. Paper Points, Size 20 PN #1560, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code EKN·August 4, 2017

    Ultradent Products, Inc. Paper Points, Size 50 PN #1559, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins..

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code EKN·August 4, 2017

    Point, Paper, Endodontic

    FDA classification
    FDA Class 1 ·Point, Paper, Endodontic

    Pro-Eko Srl

    Manufacturer
    🇮🇹 Italy·3 Basic UDI-DIs·8 Devices

    EKU Elektronik GmbH

    Manufacturer
    🇩🇪 Germany

    EKF-diagnostic GmbH

    Manufacturer
    🇩🇪 Germany

    Eko Health, Inc.

    Manufacturer
    🇺🇸 United States·2 Basic UDI-DIs·2 Devices·Eurofins Electric & Electronics Finland Oy

    Lab Scanner

    FDA UDI
    3shape A/S·05902729750417·Digital impression lab scanner for CAD/CAM

    Lab Scanner

    FDA UDI
    3shape A/S·05902729750424·Digital impression lab scanner for CAD/CAM

    EKF Life Sciences

    FDA registration
    EKF Life Sciences·3 products·🇺🇸 United States

    EKF DIAGNOSTIC GMBH

    FDA registration
    EKF DIAGNOSTIC GMBH·4 products·🇩🇪 Germany

    Eko Health, Inc.

    FDA registration
    Eko Health, Inc.·5 products·🇺🇸 United States

    BK-N

    FDA UDI
    BIOTRONIK SE & Co. KG·04035479144777·

    EKF Link

    FDA UDI
    EKF-diagnostic GmbH·04048534002011·EKF Link is a data and device management system...