BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    SERUM CROSSLAPS ONE STEP ELISA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Synchro2 Support Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMARIS GINGIVA OPAQUER

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNCHRO2-14 SUPPORT STRAIGHT 215CM

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·December 14, 2023

    XIA 3 TITANIUM POLYAXIAL SCREW DIA 7.5 X 70 MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-SWITZERLAND·Product code MNH·March 5, 2013

    SPRINT

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 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