BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517967169·Brigade Lateral, 11x34x32mm 30°

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972176·posteriors; shade BL2; size S; upper jaw

    CYSTIC FIBROSIS TESTING INSTRUMENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Parkell Universal Adhesive

    FDA 510(k)
    FDA Class 2 ·Dental

    ZILVER PTX DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·August 28, 2014

    ENDOPATH TRISTAR EXTRAPERITONEAL DISSECTOR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·May 4, 1997

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·February 21, 2013

    RENEGADE HI-FLO MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRA·January 27, 2011

    MINILINK TRANSMITTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 31, 2014