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

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    EASYRA CK-MB REAGENT, EASYRA CRP REAGENT, EASY CAL CRP CALIBRATOR KIT, EASYQC CRP QUALITY CONTROL MATERIAL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694033619·Plate, 3mm, Lefort I, 1.6mm, Left

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981175771·Z-Rod, Dia. 6.0mm, Titanium, 80mm

    Stryker

    FDA UDI
    Provision·B504OM5130080030S30·

    Stryker

    FDA UDI
    Provision·00810041060495·

    Stryker

    FDA UDI
    Provision·B504OM51300800300·

    NA

    FDA UDI
    STRYKER CORPORATION·07613154080465·4.7mm Barrel

    NA

    FDA UDI
    STRYKER CORPORATION·04546540079664·3.2mm x 18.3mm Metal Cutting Heliocoidal Rasp

    ALBOGRAFT VASCULAR PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPROCESSED TROCARS, MODEL B5LT AND CB5LT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HELIOCOIDAL RASP.

    FDA Adverse Event
    Malfunction ·ORCHID UNIQUE·Product code HBE·February 21, 2020

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP·Product code DTQ·May 21, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 30, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 16, 2011

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 15, 2024

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 12, 2026

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 22, 2020