BEUDAMED
    12 results · 17ms · Sources: EU EUDAMED, US FDA

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    CUFF CONNECTOR

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517360816·CoRoent SI Rasp, 12x17x14mm

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515204232·Locking Pliers, small tip 7mm wide, 6 3/4"

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790148000·discovery® Bracket with hook, - 7° Torque, 0° A...

    SERUM, B1A GLOBULIN C3C GOAT ANTI-HUMAN

    FDA 510(k)
    FDA Class 2 ·Immunology

    PROGUIDE CHRONIC DIALYSIS CATHETER

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

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·May 5, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    LOCKING DRIVER FOR CSLP

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code LXH·August 3, 2010

    BD ALARIS¿ EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026