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

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    Ziehm Vision RFD

    FDA 510(k)
    FDA Class 2 ·Radiology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776181932·Bruns Curette hollow hdl str oval

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780183815·Integra® Jarit® Bruns Oval Cup Curette, 6-3/4",...

    Stryker

    FDA UDI
    Barco, Inc.·00700621719564·VGA/RGB to HDMI Converter

    Stryker

    FDA UDI
    Barco, Inc.·00700621719571·3G-SDI to HDMI Converter

    Stryker

    FDA UDI
    Barco, Inc.·00700621719588·DVI to HDMI Converter

    Stryker

    FDA UDI
    Barco, Inc.·00700621719557·S-Video/Composite to HDMI Converter

    BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LIGHTHOUSE URINARY CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Connected OR Cart

    FDA UDI
    STRYKER CORPORATION·00858701006360·.

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056242·Multi-Specialty Cart Pull-Out Shelf with Pin Rails

    Neurotech

    FDA UDI
    STRYKER CORPORATION·07613327628319·

    Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qty 1, Rx Only, Manufactured for: Stryker, 5900 Optical Court, San Jose, CA 95138, UDI: 07613327462784 - Product Usage: The Connect OR Cart is a mobile, medical-grade cart intended to store and transport components of minimally invasive and open-field imaging systems such as the Stryker Advanced Imaging Modality (AIM) System, PINPOINT Endoscopic Fluorescence Imaging System, or SPY Portable Handled Imaging (SPY-PHI) System) during intraoperative use. The Cart also provides power, video, and data connections to the components.

    FDA Recall
    Terminated ·Stryker Corporation·Product code BZN·April 23, 2019

    Stryker brand Cart with Isolation Transformer, Model Numbers: 240-099-001, 240-099-001K, 240-099-011, 240-099-011K, 240-099-020, 240-099-020K, 240-099-050, 240-099-072. 240-099-001, 240-099-001K, 240-099-011, 240-099-011K, 240-099-020, 240-099-020K, 240-099-050, 240-099-072, Product is manufactured and distributed by Stryker Endoscopy San Jose, CA The product is indicated for use in the carts include an isolation transfer and a power cord for connecting the transformer to an electrical outlet as means of providing power to the cart for the equipment it houses.

    FDA Recall
    Terminated ·Stryker Endoscopy·Product code GCJ·April 16, 2010

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 28, 2026

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 21, 2026

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 20, 2026

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·November 4, 2014