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

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    OsteoFab Patient Specific Cranial Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    MAESTRO TOTAL WRIST

    FDA UDI
    Biomet Orthopedics, LLC·00880304269026·

    Maestro™ Total Wrist

    FDA UDI
    Biomet Orthopedics, LLC·00887868239373·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694016087·Bur Hole Shunt Plate, Extended Hole

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306821363·Bi-Polar Yasargi Forceps, Bayonet, 2-Pin Connec...

    SNAP MODEL 8 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FLAATZ 750

    FDA 510(k)
    FDA Class 2 ·Radiology

    RD SET YI

    FDA Adverse Event
    Malfunction ·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021

    RD SET DCI

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023

    BD LUER-LOK¿ TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·December 8, 2021

    MENICON ASRB (ASMOFILCON A) SILICONE HYDROGEL SOFT CONTACT LENS

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·March 18, 2026

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·February 25, 2025

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 14, 2025

    RSP SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code KWS·June 13, 2013

    WALLSTENT BILIARY ENDOPROSTHESIS

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·July 27, 2011

    PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·September 26, 2008

    RD SET

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·December 31, 2025

    RD SET

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·December 31, 2025

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·May 20, 2024

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·October 25, 2023