BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    TMR48

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Generic Buccal Tubes

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746153808·DB TUBE INCONEL LR 2ND MOL 022 T-10 R=0 3MM W/HK

    PICO-K

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GENGIGEL MOUTHRINSE

    FDA 510(k)
    FDA Unclassified ·Unknown

    RADIOLUCENT INSRT H&LE FOR EXPERT NL/100

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·October 1, 2021

    DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·February 9, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·January 8, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·July 24, 2019

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·October 1, 2021

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·May 25, 2023

    THERMA CARE

    FDA Adverse Event
    Injury ·PROCTER & GAMBLE PAPER PRODUCT CO·Product code IMD·March 6, 2002

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026