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

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    VMA BY HPLC TEST (VANILMANDELIC ACID)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NC Mono Scanbody

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600380580·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694032858·EnCompass 10mm Drill Guide

    Rib Retractor

    FDA UDI
    KOROS U.S.A., INC.·10840199536198·Rib Spreader Pediatric Size 3, 3-1/8" Arm Lengt...

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981127466·No profile DTS Guide 10mm

    n/a

    FDA UDI
    Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM51008613140101·Rotary diamond instrument for dental application

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108055·MCPHERSON NEEDLE HOLDER STRAIGHT

    GC Ortho Chain

    FDA UDI
    Gc Orthodontics America Inc.·E53586101000011·GC ORTHO CHAIN Clear Short

    GC Ortho Chain

    FDA UDI
    Gc Orthodontics America Inc.·D78886101000001·GC ORTHO CHAIN CLEAR SHORT 2M

    GC Ortho Chain

    FDA UDI
    Gc Orthodontics America Inc.·E53586101000001·GC ORTHO CHAIN CLEAR SHORT 2M

    HICP200 Patient/Monitor Interconnect Cable

    FDA 510(k)
    FDA Class 2 ·Neurology

    FUTURE MOBILITY HEALTHCARE INC. ORION II WHEELCHAIR AND STELLATO MECHANICAL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    TUBING SET

    FDA Adverse Event
    Malfunction ·Product code DTZ·April 14, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 10, 2014

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·October 7, 2010

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·June 23, 2015

    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012