BEUDAMED
    8 results · 19ms · 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 ×

    DenMat Bulk Fill Composite

    FDA 510(k)
    FDA Class 2 ·Dental

    SELEC-3 I.V.ADMINISTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Fundus Camera

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GOLD-TITE® SQUARE UNISCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·September 13, 2021

    BD BBL¿ GRAM SAFRANIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code JTS·January 23, 2026

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 9, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013