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

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    Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821607750·CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

    Sterile ACIF PEEK

    FDA UDI
    Tyber Medical, LLC·M6958101607750·ACIF - 16mm x 7mm x 7.5 deg PEEK Curved

    POWDER-FREE LATEX PATIENT EXAMINATION GLOVE,WITH EXTRACTABLE PROTEIN CONTENT LABELLING CLAIM (50 MICROGRAM PER GRAM OF

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BD INTIMA II CLOSED IV CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 4, 2025

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 10, 2010

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·December 10, 2010

    CORTSCR Ø3.5 L20 TI

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·June 11, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 7, 2011

    VERSASTEP 5MM SGLUSE DILT/CANN W/EXPSLV

    FDA Adverse Event
    Malfunction ·PONCE - USS·Product code GCJ·September 8, 2008

    UNKNOWN IV CATHETER

    FDA Adverse Event
    Injury ·BD (SUZHOU)·Product code FOZ·January 13, 2016

    ESSURE

    FDA Adverse Event
    Injury ·BAYER HEALTHCARE LLC·Product code HHS·September 14, 2016

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·December 10, 2010

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 2, 2010

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 17, 2010

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·December 10, 2010

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·December 10, 2010

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 2, 2010