BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    DUAL GUIDE INTRODUCER CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756284974·LATEX SAFE STD C-SECTION

    PERINATAL COMPUTER SYS MODEL 100A & 100B

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BEHRING POLAROID OPUS THEOPHYLLINE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024143494·

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024143524·

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024143500·

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024143517·

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code LPH·June 25, 2014

    SOL 13.5 STD 8.0 FULL PC 12/14

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·November 5, 2010

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 3, 2013