BEUDAMED
    24 results · 19ms · Sources: EU EUDAMED, US FDA

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    VENTRESCREEN MITE/MOLD ALLERGY TEST KIT ENZYME IM.

    FDA 510(k)
    FDA Class 2 ·Immunology

    FUSE ™ SPINAL SYSTEM

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169245716·DISTRACTOR 2870009 DISTRACTOR 9MM

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556702410·GC Initial™ MC Paste Opaque OB4, 3g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228700091·GC Initial™ MC Paste Opaque OB4, 3g

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989051827·UPPER LEFT SECOND MOLAR TRIMLINE BAND SIZE 9

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707032885·WEB 1ST MOLAR BANDS n.LL 9

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867313781·Driver Shaft, T4, Self Retaining,Mini AO

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 12, 2021

    Lens, Contact (Polymethylmethacrylate)

    FDA Pre-Market Approval
    FDA Unclassified ·3M FLUOROPOLYMER CONTACT LENS (FLUROFOCON A)

    Esophageal Cooling Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AT HOME DRUG TEST MODELS, 9308T AND 9308X

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    Y-PLATE, 1.6MM, 6 HOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·June 14, 2021

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·October 11, 2024

    DRIVER SHAFT, T4, NON-RETAINING, MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 20, 2022

    DRIVER SHAFT, T4, NON-RETAINING, MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 3, 2024

    VA LOCKING SCREW, 1.4X8MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·July 3, 2024

    DRIVER SHAFT, T4, SELF RETAINING,MINI AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 3, 2024

    VA LOCKING SCREW, 1.4X9MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·September 2, 2020

    MONOPOLAR CURVED SCISSORSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 12, 2014