BEUDAMED
    11 results · 20ms · 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 ×

    SR ANTARIS ANTERIOR TEETH/SR POSTARIS POSTERIOR TEETH

    FDA 510(k)
    FDA Class 2 ·Dental

    MILLENNIUM

    FDA UDI
    Avalign Technologies, Inc.·00190776331313·Castroviejo Needle Holder

    Xpert Xpress Flu, Xpert Nasopharyngeal Sample Collection Kit, GeneXpert Dx Systems (GX-I, GX-II, GX-IV, GX-XVI), GeneXpert Infinity-48 System and GeneXpert Infinity-48s System, GeneXpert Infinity-80 System

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NOVASPINE POWERED SUCTION PUMP PRO-1

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

    CERENOVUS ENTERPRISE

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·December 11, 2024

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·February 14, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 29, 2014

    CERENOVUS ENTERPRISE

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code NJE·December 2, 2025

    PROWLER SELECT

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRA·December 11, 2024

    CERENOVUS ENTERPRISE

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·February 11, 2026