BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Clover 50/Clover60/Clover70 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868310881·

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304256897·

    KIT BD MAX ENTERIC VIRAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCH·March 31, 2022

    OSSIX BONE, OSSIX PLUS

    FDA Adverse Event
    Injury ·DATUM DENTAL LTD.·Product code NPM·June 22, 2022

    GRYPHON PEEK DS ANCHOR W/ ORTHOCORD, GRYPHON PEEK ANCHOR W/ ORTHOCORD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AVAULTA SUPPORT SYSTEM/AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    5MM, 45CM L-TIP ELECTROSURGICAL PROBE (3BX)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·October 10, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 11, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDJ·October 21, 2015