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.

    DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331134968·caroll tendon pulling forceps, curved shaft, al...

    SCENTED MENSTRUAL PAD

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NUCLEOTOME

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MENTOR MEMORYSHAPE BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·June 10, 2019

    ENDURON NEUT 56 OR 68ODX26ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDL·June 25, 2014

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·November 4, 2010

    PELVISOFT ACELLULAR COLLAGEN BIOMESH

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABS·Product code FTM·December 27, 2012