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

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    Second Opinion® BLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    Syntec-Taichung Non-sterile Bone Plate and Screw Implants

    FDA UDI
    SYNTEC SCIENTIFIC CORPORATION·04719864685082·Mini T-Plate 2.0 x Head 3Holes x Shaft 9Holes

    devemed

    FDA UDI
    devemed GmbH·04061644038633·Suction cannula Ø 3.0mm | 20.0cm 90° | with slo...

    TAPERLOC COMPLETE RASP/PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304632585·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A243230120·24mm H x 32mm W x 30mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A243230150·24mm H x 32mm W x 30mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A24323080·24mm H x 32mm W x 30mm L x 8 degrees ALIF

    Reicodent

    FDA UDI
    devemed GmbH·04061644061617·Suction cannula Ø 3.0mm | 20.0cm 90° | with slo...

    Palladian Lumbar Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VITEK GRAM NEGATIVE SUSCEPTIBILITY (GNS) CARD FOR ERTAPENEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·December 19, 2024

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·December 19, 2024

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·December 19, 2024

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·December 19, 2024

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·December 19, 2024

    NEXUS® BONESCALPEL® 20MM, BLUNT BLADE + IRRIGATION TUBING KIT

    FDA Adverse Event
    Malfunction ·MISONIX, INC.·Product code LFL·December 19, 2024

    BD LUER-LOK¿ SYRINGE STERILE, SINGLE USE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·February 2, 2023

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·November 7, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·September 1, 2011

    PDS CORD

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code NEW·July 23, 2013