BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    AURAFLEX PROGESTERONE 150TEST PACK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517700803·BASE Ti HL Implant, 6x34x24mm 30°

    SUPER VIEW DISPOSABLE BIOM LENS SET

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    G.o.c.c.l.e.s.

    FDA 510(k)
    FDA Class 2 ·Dental

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·VYGON·Product code FOS·February 17, 2021

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·January 6, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014