Fluoroplastic Offset Total Prosthesis (TORP)

Fluoroplastic Offset Total Prosthesis (TORP)

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Fluoroplastic Offset Total Prosthesis (TORP)

Otology

E2142

Fluoroplastic Offset Total Prosthesis (TORP)

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Fluoroplastic Offset TORP designed for total ossicular reconstruction, providing stable support and efficient sound transmission for hearing restoration.

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    • Head: The head plate or disk is the part that is placed against the tympanic membrane. It is designed to provide stability and support for the device.
    • These devices can be made using fluoroplastic material. Fluoroplastic is a non-reactive and low-friction material that can be used for coating or lining certain parts of the device.

    Design Benefit:

    The Middle ear implants restores or improves the hearing ability by providing structural support to ossicular chain thereby maintaining stability of middle ear resulting in effective sound transmission which enhances speech perception.

    Duration of Use: 

    Long-term use (Normally intended for continuous use for more than 30 days) 

    Intended Purpose: 

    Middle ear implants are used to reconstruct, provide structural support to the ossicular chain (i.e., Incus, Malleus & Stapes) facilitating stability in the middle ear resulting in improved hearing.

    Clinical Indications

    • Immobility of ear bones (Malleus, Incus and Stapes). 
    • Otosclerosis/congenital stapes fixation and malleus fixation. 
    • Traumatic injury to the ossicles. 
    • Chronic otitis media with conductive hearing loss. 
    • Malformation of the middle ear. 
    • Revision surgery due to insufficient hearing improvement as may be caused by prosthesis dislocation. 
    • Revision operation on a mal-positioned prosthesis

    Performance Characteristics

    • Middle Ear Implants (MEIs) are medical devices designed to restore the function of the middle ear or enhances the conduction of sound in cases where there are pathologic changes affects the conductive hearing mechanism. 
    • MEIs transmits sound effectively from the tympanic membrane to the inner ear. 
    • MEIs should be securely fixed in place to ensure stability and long term functionality. 
    • The MEIs replaces ear bones(stapes, incus, malleus) which are part of the natural ossicular chain. It's design facilitates secure attachment of the bones and oval window. 
    • MEIs come in various sizes and shapes to accommodate the anatomical variations of the patients. The appropriate sizes and shapes should be selected to ensure a proper fit and optimal sound transmission.
    • MEI remains stable within the middle ear and is capable of withstanding the mechanical stresses associated with normal middle ear function. 
    • MEI are easy to insert during the surgical procedure. It has a smooth surface and a shape that allows for smooth insertion without causing trauma to the delicate structures of the middle ear.

    Safety Information & Contraindications

    Safety

    • The device is for single use only. Do not re-sterilize or re-use.
    • Do not re-sterile- if the device is resterilised, it may cause harm or infection to patient due to re-sterilization of the device.
    • The ENT surgeon is encouraged to carefully choose Middle ear Implant size and material to meet the needs of each specific clinical situation, while minimizing adverse effects.
    • Do not use if the packaging has been opened or damaged.
    • The Titanium Middle Ear Implant have been determined to be MR conditional. Material is safe up to 1.5 T in Magnetic field.

    Contraindications

    • Acute otitis media, which can cause implant displacement 
    • Acute and chronic infectious diseases 
    • Known wound healing disorders
    • Dislocated, fractured or fixed stapes footplate and hyper mobile stapes footplate (“Floating Footplate”) 
    • Treatment with cytotoxic drugs or radiotherapy (e.g., for malignant tumour)
    • Particular material allergy 
    • General impairment of wound healing 
    • Patient suffering from alcohol, drug, or nicotine abuse 
    • Medical issues surrounding the middle ear implant surgery

    Material: Fluoroplastic (1 Unit/Box, ETO Sterile)

    Ref.
    Number
    Shaft Dia.
    OD/ID
    Disk
    Diameter
    Functional Length Total
    Length
    E2142
    0.8 - 7.00 - 3.00 7.00


    All measurements are in mm

    Special Instructions

    Provide any specific requirements or notes related to your order. Our team will review and accommodate where possible.

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    Frequently Asked Questions

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    Still have questions?

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    +61 410 737 246

    info@eonmeditech.com.au

    Who is this product intended for?

    This product is designed for use by healthcare professionals and/or individuals, depending on its intended application. Please refer to the product details or consult a medical professional if unsure.

    Is this product suitable for home use?

    Some products are designed for home use, while others are intended for clinical environments. Check the product specifications to confirm suitability.

    Are your products compliant with quality standards?

    Yes, all products are manufactured under internationally recognized quality systems and aligned with applicable regulatory requirements.

    How do I use this product correctly?

    Each product includes usage instructions or guidance materials. For best results, follow the instructions carefully or consult a healthcare professional.

    Do you offer bulk or institutional purchasing?

    Yes, we support bulk orders for clinics, hospitals, and distributors. Please contact our sales team for more information.

    What is the delivery timeline?

    Delivery times vary based on location and availability, but we aim to fulfill orders within standard Australian shipping timelines.

    What should I do if I need support or face an issue?

    If you need assistance, our support team is available to help with product guidance, troubleshooting, or order-related queries.

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    info@eonmeditech.com.au

    +61 410 737 246

    81a Eggleton Street, Blacktown, NSW 2148, AU