BEUDAMED
    10 results · 21ms · 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 ×

    Blackford Analysis Registration Product Family

    FDA 510(k)
    FDA Class 2 ·Radiology

    ZIMMER M/L TAPER HIP PROSTHESIS WITH CALCICOAT CERAMIC COATING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHETIC VINYL EXAMINATION GLOVES, POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 17, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 17, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 17, 2026

    BD MAX¿ ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·February 17, 2026

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 5, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 3, 2013

    TEGADERM CHG DRESSING

    FDA Adverse Event
    Injury ·3M HEALTH CARE·Product code FRO·June 20, 2011