BEUDAMED
    31 results · 20ms · Sources: EU EUDAMED, US FDA

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    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·STORZ MODULITH (TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·STORZ TRANSPORTABLE MODULITH SLX LITHOTRIPTER VERSION) ANSPORTABLE VERSION)

    FDA Pre-Market Approval
    STORZ MODULITH (TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·STORZ MODULITH LITHOTRIPTER, MODEL SLX FOR FRAGMENTATION OF URINARY AND UPPER URETERAL CALCULI (MOBILE VERSION)

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·STORZ MODULITH LITHOTRIPTER, MODEL SLX

    FDA Pre-Market Approval
    STORZ MODULITH (TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·STORZ TRANSPORTABLE MODULITH SLX LITHOTRIPTER VERSION) ANSPORTABLE VERSION)

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·STORZ MODULITH LITHOTRIPTER, MODEL SLX

    CC Direct CoCr Plastic Cylinder With Hex. W6mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142546·CC Direct CoCr Plastic Cylinder With Hex. W6mm

    COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH SLIM MODIOLAR ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code MCM·February 13, 2026

    Titan Modular Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556861554·FIXATION PIN

    COCHLEAR¿ NUCLEUS® NEXA® COCHLEAR IMPLANT WITH CONTOUR ADVANCE® ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·February 13, 2026

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MAXIM PFS MODEL 033-301

    Integra®

    FDA UDI
    Ascension Orthopedics, Inc.·10381780246619·Integra®Surgical Instruments The fixation pin h...

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·May 24, 2013

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·OCU-FLEX-53 SOFT CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·OCU-FLEX

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·OCU-FLEX

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·STERILIZED FINISHED OCUFILCON B LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·STERILIZED FINISHED OCUFILCON B LENSES