Goddess of the Disk Wave

MESMO Muse Goddess Wave

MESMO breast implants combine the advantages of smooth and textured surfaces, providing the best choice for women seeking natural and lasting beauty. Smooth and textured breast implants each have their own advantages, and the MESMO® finely textured implant successfully reduces the incidence of complications such as rotation, flipping, edge sensation, and deformation through its delicate texture design, especially when using teardrop-shaped implants or those larger than 350 milliliters, while still maintaining stable results.

Breast implant No. 037182 from the Ministry of Health and Welfare, commonly known as: MESMO Muse Goddess Wave

 

 

The MESMO® implants, made in Germany, focus on breast aesthetics, combining over 35 years of manufacturing experience and high-quality standards from the world-leading brand POLYTECH, offering four different projection options in round and teardrop shapes. Its micro-textured shell design promotes optimal compatibility with body tissue, reduces the risk of capsular contracture, requires no postoperative massage care, and maintains a natural breast shape for a long time.

 

POLYTECH's MESMO® implants are highly regarded in the global market and have entered Taiwan in 2023, becoming a recommended product by European doctors.

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MESMOGoddess WaveCombining the advantages of smooth and textured surfaces

Compared to smooth-surfaced breast implants, textured surface implants have fewer complications, as described by Dr. Paolo Montemurro and Dr. Vincent K.S. regarding the special requirements for patients choosing smooth-surfaced implants:

• Good organizational quality
• Implant size <350ml
• Surgical technique
• Specific postoperative care

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MESMO Muses Goddess Wave is the best choice for textured balance.

• The MESMO fine micro-textured shell combines the advantages of smooth and textured surfaces.
• MESMO can achieve the best integration with the body (capsule), requiring no post-operative massage care, presenting a true natural breast shape that lasts without displacement.
• The MESMO soft textured implant shell surface has received positive feedback due to its characteristics and ease of use, making MESMO ® suitable for various indications.
• Provides round and teardrop-shaped implants, as well as 4 types of projection: low, medium, high, and ultra-high.

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Goddess Wave Micro-textured Breast Implants

• The choice of surface material depends on the patient's needs and body structure.
• The surface of the implant affects the capsule and its formation.
• Many surgeons prefer implants with fine microtexturing to support the interaction between the implant and the tissue. This interaction is associated with a reduction in complications, such as deformation (especially for implants over 350 milliliters) as well as implant flipping and rotation.
• Smooth surface implants are associated with not adhering to body tissues, which may lead to complications over time, especially in the case of larger volumes.

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Why choose the goddess wave POLYTECH?

POLYTECH is a world-class leading brand company focused on breast aesthetics, manufacturing breast implants in Germany.

The only silicone implant manufacturer in Germany. All products are exclusively developed in Germany, and each implant undergoes very strict quality control and comprehensive testing. Over 2,000 styles of breast implants are offered to meet the needs of surgeons and the different preferences of patients.

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Goddess WaveFrom Germany | Entered Taiwan in 2023 | Recommended by doctors across Europe

• 10-year long-term comprehensive clinical safety report
• More than 35 years of complete manufacturing experience.
• +80 countries market marketing sales
• >3 million global implant sales testimony

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Why are there various types of implant surfaces?

Any foreign body around implanted tissue (including breast implants) will form a capsule. In some cases, this capsule will contract. Contraction can deform the shape of the implant and the breast. Additionally, the capsule can become very hard and cause pain. This complication is known as "capsular contracture," and its occurrence is related to the surface of the implant. The first breast implants were manufactured in the 1960s with a smooth surface. Since the mid-1970s, implants covered with micro polyurethane have been in use. Textured surface implants were introduced in the late 1980s, and there are now three different surface materials. Although breast augmentation surgical techniques have improved, the capsular contracture rate of smooth implants is 30% compared to the very low capsular contracture rate of Microthane® micro polyurethane surface implants, which is only 0-3%! Initial internal evaluations indicate that the capsular contracture rate of the minimally frictional micro-textured MESMO® surface may be similar to that of Microthane®. Compared to smooth implants (30%), the risk of capsular contracture for standard textured implants (15%) is significantly lower. For these reasons, POLYTECH specializes in implant products with micro polyurethane and textured surfaces.

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MESMO complication occurrence rate

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MESMO Muse Goddess Wave Round Model Comparison Table

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MESMO Goddess Wave Warranty Program

The extended warranty program was established in 2007, providing concrete benefits for your patients, allowing them to rest easy.

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MESMO Muses Goddess Wave allows you to create your ideal breasts at will, achieving a new realm of customization.

Everyone hopes to have their own unique beauty, and today we will introduce the MESMO® breast implant, which was newly introduced to Taiwan in 2023. It is highly recommended by European doctors and is widely praised in the global market. Not only can it help you achieve a natural and firm breast shape, but it also offers more diverse options to bring the breast shape closer to your ideal, providing a real and soft comfortable touch.

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MESMO is from Germany, with world-class technology and quality.

MESMO breast implants are manufactured by the German company POLYTECH, which has over 35 years of experience and is one of the leading brands in the field of breast augmentation materials worldwide. POLYTECH is the only company that is "Made in Germany," meaning that it develops and produces breast augmentation materials in Germany. With their innovative technology in the field of medical device manufacturing, MESMO breast implants are sold in over 80 countries worldwide and have gained the trust of over 3 million consumers.

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MESMO Muse Goddess Wave's fine texture technology: a true fusion of nature and safety

One of the highlights of the MESMO goddess breast implant is its fine textured surface technology. This design combines the advantages of smoothness and micro-texture, allowing for better integration with human tissue, ensuring stability and a natural appearance post-surgery. It will naturally conform to the chest and will not shift or deform over time.

• Natural and realistic touch: According to a survey, 94% of women reported that their breasts felt very soft after surgery, almost indistinguishable from real breasts.
• Durable aesthetic effect: The implants are designed to maintain the firmness and beauty of the breast shape for a long time, without sagging or deforming over time.
• Low risk and simple postoperative care: Unlike other surface materials of implants, the fine textured surface of the MESMO goddess wave significantly reduces the risk of capsular contracture, and there is no need for complicated massage after surgery, allowing the breast shape to maintain a natural appearance and feel.

This unique surface design also helps to avoid common complications such as edge sensation, implant flipping, and rotation, especially when using larger sizes of implants (particularly those over 350 milliliters), where the effects become particularly noticeable.

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Why do breast implants have different surface materials?

Capsular contracture is a common complication in breast augmentation surgery, which can lead to deformation of the implant and cause discomfort. This is largely related to the surface material of the implant; early implants mostly had smooth surfaces, but this increased the risk of capsular contracture. To address this issue, modern technology has developed implants with micro polyurethane and textured surfaces, which can better reduce the occurrence of capsular contracture. According to research, the Microthane® micro polyurethane surface has a contraction rate as low as 0-3%, making the postoperative results more natural and stable.

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MESMO Muses Goddess Wave offers 2 shapes and 4 projections, allowing beauty to be as desired!

MESMO provides a variety of shapes and projections, allowing for the ideal breast shape according to needs. Whether it's a natural, delicate adjustment or a pursuit of fullness and roundness, MESMO can offer suitable sizes.

2 implant shapes

• Round implant shape: The round design is suitable for women who wish for fuller and rounder breasts, especially those who want to showcase a three-dimensional curve in the upper body.
• Teardrop-shaped implants: This shape mimics the natural downward curve of the breast, making the breast shape look closer to reality, especially suitable for women seeking a natural feel.

4 types of projection

• Low projection: Suitable for women who wish to make slight adjustments to their breasts, the low projection design brings delicate changes, making the breast appearance more refined and not abrupt.
• Low, Medium, High Projection: As the projection increases, the breasts will appear fuller and more three-dimensional, meeting different levels of breast enhancement needs and helping you create the ideal breasts.

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The goddess wave has extremely high user satisfaction and safety.

Goddess breast augmentation surgery is not just about pursuing a change in appearance; safety is equally important. MESMO can ensure lasting safety after the surgery.

• Low complication rate: According to clinical data, the capsular contracture rate of the MESMO breast implants clinically shows a capsular contracture rate (Baker grade III and IV) of 0.4% to 1.2% within five years, which is far lower than other implants, allowing you to enjoy your new life after surgery with peace of mind.
• High satisfaction: 97% of users are very satisfied with the results after surgery, and 98% of users report a significant improvement or stability in quality of life.

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MESMO Muses Goddess Wave has scientifically verified safety and durability.

• Fatigue Test: MESMOGoddess WaveAfter 2 million cycles of pressure testing, simulating the dynamic pressure on the chest during daily activities, it has been proven to maintain a stable shape over the long term.
• Stretchability test: POLYTECH's implants have exceptional extensibility, capable of withstanding up to 850% extension, ensuring durability for long-term use.

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Who is suitable for choosing MESMO?

• For those who seek a natural aesthetic: If you want your breast shape to look real, natural, and feel soft after surgery, MESMO is the right choice.
• For those who are very concerned about safety: For those worried about postoperative complications, the low capsular contracture rate and scientifically proven durability of MESMO can give you peace of mind in your choice.

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Why choose MESMO?

• 35 years of world-class quality made in Germany
• Various styles, allowing beauty to be at will.
• Over 3 million successful cases worldwide.
• 10-Year Long-Term Clinical Safety Report
• Low capsular contracture rate, stable and natural effect.

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Choose MESMO, let beauty be at your fingertips!

MESMO Muse Goddess Wave has opened up more possibilities for breast augmentation surgery! In the future, we can freely create our own beautiful breast shapes like artists; whether we desire a natural and gentle aesthetic or a full and confident bust, the Muse Goddess Wave can precisely meet those needs.

If you are considering breast augmentation or have any questions or thoughts about the effects of breast augmentation surgery, feel free to contact Enherya. Together, we can achieve your beauty dreams through breast augmentation surgery!

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MESMO Muse Goddess Wave Medical Device License from the Ministry of Health and Welfare

POLYTECH breast implants, Ministry of Health and Welfare Medical Device Registration No. 037182

 

Indications

• Breast augmentation (e.g., developmental defects, underdevelopment) and plastic surgery (e.g., asymmetry, sagging, atrophy)
• Breast reconstruction (e.g.: after mastectomy)
• Implant replacement
• Combined breast and chest wall deformities (e.g., Poland syndrome, pectus excavatum, pectus carinatum)

Contraindications

In addition to the general contraindications applicable to invasive procedures, specific clinical contraindications may include:

• Patients with unstable mental states
• Repeated attempts or failures in breast contour correction
• Persistent infection conditions in clinical practice
• Systemic disease
• Immune system suppressed
• Inflammation in the implantation area
• Nervous System 1 Connective Tissue Diseases
• Expected allergic or abnormal immune reactions to breast implants
• The breast tissue to be implanted has abscesses, cysts, or tumors, as well as fibrocystic disease.
• Risk of tumor or metastatic recurrence (e.g., persistent or intermittent breast cancer)
• Severe radiation damage to the breast
• There is rib injury.
• Severe burn scars on the breast
• Insufficient tissue coverage in the implantation area (e.g., after undergoing breast reduction surgery) or reduced vascularization.
• Wound healing disorder
• Pregnancy and breastfeeding period

Warnings and Precautions

This product uses double sterile packaging. In the operating room, as long as the sterile inner packaging is not damaged or opened, the sterility of the product can be ensured. A backup implant should be available during the implantation surgery. When the sterile packaging is damaged, its sterility cannot be guaranteed. Do not use damaged breast implants. If you have any questions, please contact POLYTECH Health & Aesthetics or local medical device distributors in each country.

Avoid pollution

The surface of the implant must not be contaminated by talcum powder, dust, or skin oils. Due to static electricity, cotton fibers, talcum powder, or other surface contaminants may adhere to the implant, causing an increased foreign body reaction.
Special care must be taken to avoid contamination. Therefore, medical personnel involved in the operation should clean their sterile gloves with sterile saline solution before touching the implant.

Avoid damage during the surgical process

During the implantation surgery, care should be taken to avoid excessive force and to minimize manipulation of the implant.
When using surgical instruments near breast implants, attention should be paid to scalpels, suturing needles, and anatomical instruments. Silicone-filled breast implants may be subject to accidental mechanical trauma during the implantation or removal process. Scanning electron microscopy has observed shell ruptures on the implant shell, which may be caused by damage from instruments such as scalpels, suturing needles, injection needles, hemostatic clamps, retractors, needle holders, and forceps.
Please do not touch the implant with burning equipment.
Excessive manipulation may affect the mechanical properties of the implant, and this impact may not be detectable by the surgeon at the time of implantation.

Should follow the following suggestions

The incision should take into account the size and surface type of the implant.
Hemostasis must be carefully performed.
The size of the implant should be carefully selected. Implants of different sizes should be available to choose the appropriate size. It is recommended to use sizers during the surgical process to determine the proper size.
The pocket should match the size of the implant.
Breast implants should be placed flat on the chest and should not have any wrinkles.
It is essential to ensure that the organization has appropriate coverage, and if necessary, priority should be given to placing breast implants under the muscle.
It is advisable to avoid the direct combination of implants and medications.

Reuse and re-sterilization

Breast implants are for single use only and must not be reused or re-sterilized. The reasons are as follows:
After the implant is removed, no form of sterilization procedure on the surface characteristics of the implant is allowed or recommended.
Breast implants are very sensitive to low pressure/vacuum and may not withstand the re-sterilization procedures of medical devices.
According to international standards for the mechanical safety limits of new breast implants, it cannot be guaranteed that these limits will be met after the implants are removed, as stress is applied during the implantation and removal processes. Therefore, it cannot be guaranteed that reused products will still meet safety requirements.

Change the implant

Breast implants should never be altered before or during the implantation process. Each product should be checked for damage before implantation. Any damaged or altered products must not be used for implantation! A backup implant should be available during the implantation surgery.
Do not alter the implant, nor attempt to repair or implant a damaged implant.

Possible complications

Possible complications related to breast implants, in addition to the usual complications associated with invasive procedures, may also occur due to individual health conditions, medications, surgical techniques, and postoperative care. The following lists the intraoperative and postoperative risks associated with implants:

• Rash: The rash is characterized by redness of the skin, and its frequency depends on the different surface structures. The redness of the skin should not be confused with infection, as it usually does not accompany systemic infection symptoms and is associated with itching. The rash typically appears 7 to 10 days after implantation and can last for 2 to 3 weeks. If treatment is absolutely necessary, it is recommended to use steroids based on the literature.
• Infection: Infections associated with breast implants are very rare. Any unexplained infection occurring after implantation should be treated immediately. Antibiotics, drainage, or removal of the implant may be necessary. Bacterial cultures of wound secretions should be performed to determine the cause of the infection. Typical bacteria include: Staphylococcus aureus, Staphylococcus epidermidis, or Streptococcus. Not all infections can be treated while the breast implant remains in the body. There have been individual cases of toxic shock syndrome associated with breast implants.
• Inflammation or irritation: These are the body's responses to infection or injury, manifested as redness, swelling, or pain.
• Breast implant displacement, whether or not accompanied by persistent pain: this may be caused by improperly sized or incorrectly positioned implants. Possible causes include oversized implants, capsular contracture, and irritation caused by excessive movement of the implants. After breast surgery, pain may occur in the surgical area as well as in the chest muscle and shoulder area.
• Skin necrosis, shedding, exposure, and cracking: these complications may be caused by excessive tension on the skin from the implant (for example, the size of the implant is not compatible with the implant pocket) or interruption or reduction of blood flow to the skin (for example, trauma to the skin flap during surgery). Steroid treatment may also cause necrosis. Smokers are high-risk patients because blood circulation may be impaired. Corrective surgery may be necessary.
• Delayed wound healing: The wound healing period varies depending on the type of surgery and the location of the incision, and the healing time also differs among patients. In certain patients, especially smokers, significant delayed wound healing may occur. In this case, the risk of infection, exposure, and/or necrosis increases.
• Hematoma: A hematoma may be a precursor to infection and may increase the risk of capsular fibrosis. The occurrence of hematomas should be strictly avoided, and if a hematoma appears, it should be treated immediately. If not handled in a timely manner, significant postoperative edema or hematoma may lead to exposure or displacement of the implant. Non-absorbable hematomas may require immediate removal of the implant. Rigorous hemostasis during surgery is the best preventive measure.
• Wrinkles: Palpable implant edges or deformation may be due to differences between the implant size and the tissue pocket or insufficient tissue coverage.
• Capsular contracture or fibrosis: The fibrous tissue encapsulating the implant is a normal host response to the implant. However, this capsule may contract and harden, causing changes in the shape and position of the implant due to capsular contracture. If clinically significant (Baker III, IV) capsular contracture occurs, it may lead to aesthetic damage and pain, necessitating the removal of the implant. Closed capsulotomy is not recommended, as it may damage the breast implant. If such a procedure cannot be avoided, inspection procedures should be implemented during the surgery to prevent damage to the implant.
• Calcification: Benign calcification may occur around the implant.
• Implant rupture: Implant rupture or leakage is an absolute indication for immediate removal. The most common causes are damage to the implant during surgery (e.g., too short incisions, surgical instruments), post-surgery (e.g., punctures, biopsies, closed capsule incisions, etc.), trauma, or material fatigue. After a silicone-filled implant ruptures, the viscosity of the silicone can prevent displacement. However, there is no guarantee that the silicone will remain intact.
• Cancer risk: Epidemiological studies regarding implants show that the risk of breast cancer in women with implants is not higher than that of the control group.
• Desensitization or hypersensitivity: these may occur temporarily or permanently and may affect the breast completely or partially. Especially in cases where breast implants are inserted through an areola incision, sensation may change.
• Autoimmune and connective tissue diseases: Since the 1980s, the possible association between breast implants and these diseases has been discussed. So far, there is no evidence that breast implants cause these diseases.
• Changes in breastfeeding ability: Breast surgery may affect breastfeeding ability.
• Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL): Several studies have indicated a potential association between breast implants and the occurrence of ALCL. This means that women with breast implants may have a slightly increased risk of ALCL. Patients should be informed by the responsible surgeon about the low risk of ALCL and advised to consult their attending physician if symptoms such as seroma or swelling and pain in the implant area occur more than a year after surgery.
• Axillary lymphadenopathy
• Breast tissue/chest wall deformation: The skin covering the implant may thin due to the tension it exerts, or the pressure from the implant may deform the ribs. This may lead to the need for revision surgery.
• Impact on infants: Currently, there is no evidence to prove that breast implants pose a health risk to infants born to or breastfed by mothers with implants.
• Unsatisfactory cosmetic results: For both patients and doctors, dissatisfaction with shape or size can be minimized through careful surgical planning. Revision surgery can provide assistance, but it also comes with new risks.
• Asymmetry: The breasts present varying degrees of asymmetry in size, shape, and/or position. Pre-operative asymmetry may not be fully compensated for with implants and surgery.
• Sagging: The relaxation of breast tissue may be caused by gravity, pregnancy, weight loss, and aging. In one
• Drooping is the result of a physiological process.
• Implants may be visible: when using textured surfaces or large volume implants, as well as when there is subglandular implantation and insufficient tissue coverage, the implants may be seen.
• Silicone permeation: All modern breast implants are equipped with a special barrier layer, but it is impossible to completely eliminate the leakage of low molecular weight silicone components outside the implant shell. Typically, a small amount of silicone coexists within the tissue capsule surrounding the implant. Indeterminate granulomas are indicators for tissue examination or removal.