BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    IMACK-MB TEST PROCEDURE (MODIFICATION)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228745451·GC Initial™ Ti Opaqus Dentin ODD3, 50g

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809916493218·Multi-Axial Fenestrated Screw, Ø4.5 x 45mm, Ø6....

    POCKETIP 4414

    FDA 510(k)
    FDA Class 1 ·Dental

    CYSTINE TRYPTIC AGAR W/MANNITOL

    FDA 510(k)
    FDA Class 1 ·Microbiology

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 22, 2014

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·December 14, 2012

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010

    OSTYCUT BONE BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015