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

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    NEMIO

    FDA 510(k)
    FDA Class 2 ·Radiology

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964151491·Endo Carry-on Procedure Kit contains Intercept ...

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890106310·Zirlux 15 Degree Titanium Esthetic Abutment Pos...

    INSET II

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·January 8, 2026

    CORINNE MCCORMACK INC.

    FDA UDI
    FGX INTERNATIONAL INC.·00193033185520·

    CORINNE MCCORMACK INC.

    FDA UDI
    FGX INTERNATIONAL INC.·00193033185537·

    CORINNE MCCORMACK INC.

    FDA UDI
    FGX INTERNATIONAL INC.·00193033185513·

    STEM: M-VIZION PROXIMAL BODY 20MM L 80MM STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 31, 2021

    Intess L

    FDA UDI
    Kalitec Direct LLC·B07312K0100310·Assembly,Caddie, Lumbar Implants, Hinged

    Matira

    FDA UDI
    Kalitec Direct LLC·B073DRK010031·Drill Guide, Straight, Featureless, Amann

    Inseption

    FDA UDI
    Kalitec Direct LLC·B07314K0100310·Assembly, Caddie, ISP Implants, Hinged

    CORTEX METAMAX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    YPSOPUMP INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V·Product code FPA·April 17, 2025

    0009613348-2024-010631

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·August 12, 2024

    BD POSIFLUSH¿ NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 20, 2023

    BD POSIFLUSH¿ NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 17, 2023

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 14, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·March 1, 2011

    SPL LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008