BEUDAMED
    78 results · 21ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·HYDRACON(R) CONTACT LENSES

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200171·Max. 1. Molar band W-Fit left 17

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707027331·WEB 1ST MOLAR BANDS n.UR 17

    CC Anatomic Abutment H3mm L6mm Wide

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142218·CC Anatomic Abutment H3mm L6mm Wide

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200170101·Max. 1. Molar band W-Fit left 17

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200170501·Max. 1. Molar band W-Fit left 17

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200170051·Max. 1. Molar band W-Fit left 17

    NA

    FDA UDI
    STRYKER CORPORATION·04546540374356·4.0mm Barrel

    NA

    FDA UDI
    STRYKER CORPORATION·04546540374363·5.0mm Barrel

    NA

    FDA UDI
    STRYKER CORPORATION·07613154560509·5.0mm Barrel

    COVIDIEN PREMIUM SURGICLIP III

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FZP·February 20, 2025

    Grappler R3FLEX Stabilization System

    FDA UDI
    Paragon 28, Inc.·00889795128140·Grappler R3FLEX Single Implant Kit

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 5071 LEAD