BEUDAMED
    8 results · 18ms · 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 ×

    INTRALASE 600C LASER KERATOME

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

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993153·anteriors; shade A4; mould UCS

    FORCEPS CEV405 FENESTRATED 350MM JOHANN [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GEI·March 19, 2014

    SPIRA-C Integrated Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EMIT ETHYL ALCOHOL ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SOLETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·March 7, 2013

    2649622-2014-09473

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    PUMP,COLLEAGUE SINGLE CHANNELCOLOUR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 16, 2011