BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    HP M2376A DEVICE LINK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984194·anteriors; shade A4; mould R 66

    LATEX EXAM GLOVES (MFG: CHINA NAT CHEM CONST CORP)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PARAINFLUENZA TYPE 1 IFA TEST KIT FOR ANTI. DETECT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    6.0MM TI MATRIX POLYAXIAL SCREW 40MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code NKB·April 5, 2017

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 10, 2011

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWA·August 6, 2014

    InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.

    FDA Recall
    Terminated ·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009