BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    E100 SERIES SPO2 SENSORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970098·anteriors; shade A3.5; mould BIM

    QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ICONIX TT All Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·June 16, 2006

    ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DQY·April 29, 2014

    LIBERTY CYCLER SET, SINGLE CONN./EXT DL

    FDA Adverse Event
    Malfunction ·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FKX·February 15, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2011