BEUDAMED
    70 results · 28ms · Sources: EU EUDAMED, US FDA

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    DYNA-LINK ELITE Stand-Alone Anterior Lumbar System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Mouse anti-a-Synuclein (LB509) Concentrate, 1 mL

    FDA UDI
    LIFE TECHNOLOGIES CORPORATION·10190302000062·

    BALANCE MICROPLASTY HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304446472·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034210·Profile Zero 35mm Gap Plate

    Revelation Diamond

    FDA UDI
    Ss White Burs, Inc.·D6901802152·FG CLD1 - 5 PACK

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694065900·Profile 0 35 Gap Plate Sterile Qty 2

    CONFIRM ANTI-ESTROGEN RECEPTOR (SP1) RABBIT MONOCLONAL PRIMARY ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Hematology

    ARCHIMED REMEDY CERVICAL PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RFB VULCAN GENERATOR CE MARK

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GEI·August 4, 2017

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 12, 2016

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·February 7, 2022

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 12, 2016

    TSRH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 27, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 12, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·November 17, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 1, 2022

    VULCAN GENERATOR, CE MARK

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GEI·August 26, 2015

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 22, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·June 13, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 27, 2024