BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    MYOCARD BIOPSY FORCEP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517310484·Archon Screw, 4.0x12mm S.T. Variable

    NA

    FDA UDI
    STRYKER CORPORATION·07613327055528·[Cutting Loop Electrode, .012 wire, 27 Fr ¿ 30 ...

    PLUM A+ HYPERBARIC INFUSION SYSTEM WITH HOSPIRA MEDNET SOFTWARE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VITEK MS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NDEHP PRIMARY PLUM PREPIERCED Y

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·April 25, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 18, 2014

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS,INC.·Product code HQL·October 7, 2010

    EXCLAIM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 17, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021