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

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    BHDENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517563644·CoRoent Ant TLIF PEEK, 10x13x28mm 0°

    Dornier MedTech

    FDA UDI
    Dornier MedTech GmbH·04049957003135·Gemini Lithotripter, 50 KW

    Dornier MedTech

    FDA UDI
    Dornier MedTech GmbH·04049957003265·Gemini Lithotripter, 65 KW

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114285·LACRIMAL CAN TAPPERED 19/23GA

    HAND SURGERY OSTEOTOME

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896052529·HAND SURGERY OSTEOTOME STRAIGHT BLADE

    VARIANT II TOTAL GHB

    FDA 510(k)
    FDA Class 2 ·Hematology

    STERILOX LIQUID CHEMICAL STERILANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    GENTEEL HOMECARE PRODUCTS·Product code ITJ·May 9, 2013

    R3 3 HOLE HA CTD ACET SHELL 56MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·September 19, 2014

    UNICEL® DXC 600I SYNCHRON ® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·May 26, 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 FX25 OXYGENATOR

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

    CAPIOX FX05

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 21, 2020

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 1, 2022

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 16, 2022

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·November 17, 2023