BEUDAMED
    263 results · 31ms · Sources: EU EUDAMED, US FDA

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    Picowon

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NA

    FDA UDI
    Stryker GmbH·07613154639588·Screw Marker 14,6

    16PW - Krispy Kreme FAK - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015064·16PW - Krispy Kreme FAK - Poly White

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113431·CRESCENT KNIFE DOUBLE BEVEL (BX/5)

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383556279·"An absorbent paper points is an endodontic pap...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450157381·

    HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·June 13, 2014

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·September 3, 2014

    UNIVERSAL GIA 12MM

    FDA Adverse Event
    Malfunction ·COVIDIEN UNITED STATES SURGICAL CORPORATION·Product code GDW·September 15, 2009

    TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code LOX·June 26, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·April 1, 2014

    ENDURANT BIFURCATED STENT GRAFT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·February 2, 2017

    TRUERESULT

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·April 9, 2015

    XIENCE ALPINE EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·March 28, 2016

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·August 3, 2011

    ACUVUE BRAND CONTACT LENSES (NON-SPECIFIC)

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 28, 2013

    ALLEVYN CAVITY 12 X 4CM TUBULAR CTN 5

    FDA Adverse Event
    Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code NAD·August 21, 2015