- The flexible loop, typically made of fluoroplastic, acts as a connector between the incus (a small bone in the middle ear) and the oval window (a membrane-covered opening leading to the inner ear). It provides a flexible and adjustable connection between these two structures.
- The piston is another important component of the attachment. It is usually made of the same materials as the flexible loop and serves as a connector between the loop and the oval window. The piston is designed to transmit sound vibrations efficiently from the incus to the oval window, ensuring proper sound transmission to the inner ear.
- The device can be customized by a doctor according to the specific needs of a patient. The doctor has the ability to trim the device, adjusting its length or shape to optimize its performance and fit for the individual patient.
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: CP Titanium Medical Grade ASTM F 67 & Fluoroplastic (PTFE) (1 Unit/Box, Gamma Sterile)
| Ref. Number |
Shaft Diameter |
Functional Length |
Total Length |
|---|---|---|---|
| E4119 |
0.40 | 7.00 - 4.00 | 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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Common Questions
Frequently Asked Questions
Have a question not covered here? Our team is ready to help, reach out via email or phone and we'll get back to you within one business day.
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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+61 410 737 246
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