BEUDAMED
    132 results · 23ms · Sources: EU EUDAMED, US FDA

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    MUST LT 25MM LONG - PEDICLE SCREW Ø6X45 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·January 19, 2024

    M.U.S.T. Pedicle Screw Extension and Long Tab Implants

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MUST LT 03.57.035 MUST LT 15MM SHORT - PEDICLE SCREW Ø7X45 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 18, 2022

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·September 18, 2025

    PEDICLE SCREW MUST LT 15MM SHORT - PEDICLE SCREW Ø4.5X30 CANN

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 8, 2023

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·July 16, 2025

    MUST LT 03.59.234 MUST LT 25MM LONG - PEDICLE SCREW Ø7X40 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·February 16, 2022

    MUST LT 15MM SHORT - PEDICLE SCREW Ø8X40 CANN

    FDA Adverse Event
    Death ·MEDACTA INTERNATIONAL SA·Product code NKB·March 29, 2023

    MUST LT MUST LT 25MM LONG - PEDICLE SCREW 6X45 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·July 7, 2021

    MUST LT MUST LT 15MM SHORT - PEDICLE SCREW Ø6X40 CANN

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 3, 2021

    MECTALIF OBLIQUE (TI PEEK) TIPEEK 10X24X10 L5°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·June 25, 2024

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114094·SIMCOE CORTEX EXTRACTOR 23GA 0.4MM PK/10

    Poly Stim II

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00850958007428·1.25" Round Foam

    Poly Stim II

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·10850958007425·1.26 Round Foam, Case of 10

    Medical Science Products Private Label

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00092237900468·1.25" Round Foam

    PROCLUDE-SENSITIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    AURA 20 BIPOLAR ELECTROSURGICAL COAGULATOR, MODEL 26-2500

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 17, 2008

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·August 11, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013