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

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    AAA Model

    FDA 510(k)
    FDA Class 2 ·Radiology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047588·RELINE-O Trial, 7mm H Ang Left L-pop

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006030·A3

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180172425·LONG ADAPTER FOR VALTCHEV UTERINE MOBILIZER

    Collin-Duval Intestinal Clamp

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896120136·Collin-Duval Intestinal Clamp Serrated

    DOYEN SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896083820·DOYEN SCISSORS CURVED SERRATED BLADES POWER CUT...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694007238·M4 Mini Plate Organizer, Series II

    SPIFE CHOLESTEROL PROFILE KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CRPEX-HS C-REACTIVE PROTEIN LIT ASSAY, CATALOG NO. 1010

    FDA 510(k)
    FDA Class 2 ·Immunology

    B BRAUN

    FDA Adverse Event
    Other ·B BRAUN·Product code FPA·August 31, 2006

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·March 26, 2008

    MINICAP PD TRANSFER SET (EASY-LOCK) WITH TWIST CLAMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·May 11, 2006

    BD

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code NBW·September 3, 2005

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    D-TRONPLUS POWER PACK

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·October 7, 2008

    LAMITRODE 44C LEAD KIT 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·December 20, 2016

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·June 20, 2012

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 24, 2014

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    DA+ T SERIES SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·August 11, 2011