BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    SLT 28MM XXL FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517701169·BASE Ti HL Implant, 10x42x30mm 25°

    Spinous Process System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981129705·Plate Inserter, Spinous Process Spacer

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867055124·PLATE, POW, LOCKING, TI, 2.5 MM

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127023941·Stem Acetate Kit

    Turbett Surgical Container

    FDA 510(k)
    FDA Class 2 ·General Hospital

    JOSTRA HLM TUBING SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNCRA CRT-P

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·February 9, 2013

    RENAL-DISPOSABLE

    FDA Adverse Event
    Malfunction ·Product code FKX·January 7, 2011

    ROTAWIRE? AND WIRECLIP? TORQUER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (HEREDIA)·Product code MCX·July 23, 2014