BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ProGear® Surgical Mask with Oxafence®, Model AV82030

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

    BD BBL™ Taxo™ TB Niacin Test Strips

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902317418·BD BBL™ Taxo™ TB Niacin Test Strips

    BD BBL¿ TAXO¿ TB NIACIN TEST STRIPS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code JTO·July 12, 2023

    Gabriel 3 Way EnFit Valve

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

    MEDLEY ETCO2 MODULE (INCLUDES ACCESSORIES), MODEL 8300

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 7, 2019

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·October 14, 2014

    LACTOSORB SCREW 2.0X7MM 2 PACK

    FDA Adverse Event
    BIOMET MICROFIXATION·Product code HWC·September 1, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 17, 2013

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·July 30, 2018