BEUDAMED
    15 results · 23ms · 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 ×

    PEDIGUARD NERVE DETECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00812564032942·OPTHAMOLOGY GOWN/TWL PACK

    ArgenZ ST 98x14 ML OM2

    FDA UDI
    ARGEN CORPORATION, THE·D818123390·Dental porcelain/ceramic restoration kit

    AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 39cm x 130°

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016673·

    LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)

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

    MY BREAST FRIEND, BREAST SELF-EXAM PAD

    FDA 510(k)
    FDA Class 1 ·Radiology

    MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·April 10, 2020

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·April 10, 2020

    ETHILON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·April 10, 2020

    DERMABOND UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code EXM·April 10, 2020

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·April 10, 2020

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·April 10, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·June 10, 2011