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

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    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·PowerLook® Tomo Detection Software

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528126448·2.0/2.4/3.0/4.0mm Screw Extractor

    Humeris Shoulder

    FDA UDI
    FX SOLUTIONS·03701037301548·HUMERIS STEM TA6V SIZE 09 CEMENTLESS Ti/HA

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022644·KLEOS PSL METAL MBT 022 LL12-LR12 PK5 UNI

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707016854·CALIBRA 1ST MOLAR BANDS n.LR 9

    18mm Cervical Plate with Cover Plate for 9mm Interbody

    FDA UDI
    XENCO MEDICAL LLC·B064XM21600091·

    18mm CERVICAL PLATE FOR 9mm INTERBODY

    FDA UDI
    XENCO MEDICAL LLC·B064XM31600091·

    18mm CERVICAL PLATE FOR 9mm INTERBODY

    FDA UDI
    XENCO MEDICAL LLC·B064XMPH31600091·

    2.0/2.4/3.0/4.0MM SCREW EXTRACTOR

    FDA Adverse Event
    Malfunction ·OSTEOMED, LLC·Product code HWC·July 15, 2024

    ABL90 FLEX ANALYZER

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code JGS·September 25, 2018

    MOBI-C IMPLANT M "STANDARD" 15X17 H4.5

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MJO·April 22, 2020

    Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)

    FDA Pre-Market Approval
    FDA Class 2 ·AXSYM CORE-M 2.0 AND AXSYM CORE-M 2.0 CONTROLS

    Mitral Valve Repair Devices

    FDA Pre-Market Approval
    FDA Class 3 ·MITRACLIP DELIVERY SYSTEM

    MOBI-C P&F IMPLANT 19X19 H05

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MJO·February 4, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 10, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 13, 2011

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 12, 2008

    MOBI-C IMPLANT M"STANDARD" 15X19 H5

    FDA Adverse Event
    Malfunction ·LDR MÉDICAL·Product code MJO·July 11, 2022

    MOBI-C P&F IMPLANT 17X19 H5

    FDA Adverse Event
    Injury ·LDR MÉDICAL·Product code MJO·March 17, 2020

    MOBI-C IMPLANT; SIZE UNKNOWN

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MJO·January 22, 2026