BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    NEOLON NEOPRENE SURGICAL GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517701510·BASE HL Trial, 14x34x24mm 25°

    TRICON UNICOMPARTMENTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COAG-1 PT-NC TEST CARD

    FDA 510(k)
    FDA Class 2 ·Hematology

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004655295432517201·BTE-TRT

    TPRLC 133 MP TYPE1 PPS SO 11.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·July 14, 2021

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·February 11, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·December 13, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014