BEUDAMED
    10 results · 38ms · 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 ×

    DS N95 SURGICAL MASKS AND FLAT SURGICAL

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

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036027209·

    LumaFlex Double J stent, 2 open tips, Ch/Fr6/L.28cm, without wire

    FDA UDI
    Promepla·03700512967521·

    PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB

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

    QUICKSCREEN PRO MULTI DRUG SCREENING TEST, MODEL 9153 PAT04

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·May 28, 2025

    HIGH FREQUENCY VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 11, 2010

    FORTIFY ST DR, DF4 CONNECTOR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 2, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 15, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·May 16, 2011