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SKU 10092

Belotero Volume Lidocaine

Còn hàng
Dung tích
2 x 1 mL
Nhà sản xuất
Merz Aesthetics
Xuất xứ
Thụy Sĩ
Giá bán sỉ và lịch sử giá chỉ dành cho tài khoản đã xác minh
allpara cung cấp sản phẩm cho người hành nghề có giấy phép. Đăng nhập hoặc đăng ký tài khoản B2B để xem giá theo thời gian thực, các mức giá theo số lượng và lịch sử giá.

Belotero Volume Lidocaine by Merz Aesthetics is the volumising grade of the BELOTERO range, a hyaluronic acid dermal filler supplied with lidocaine in the syringe and developed for severe nasolabial folds and to enhance the cheeks, the temples and the chin. Injection is into the deep subcutaneous layers or on top of the periosteum, with effects lasting up to 18 months in the nasolabial folds and up to 12 months in the cheeks, temples and chin. Each 1 mL contains sodium hyaluronate 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), and lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7, which makes it the most concentrated grade in the range. Belotero Volume filler is supplied as 2 x 1 mL, a two-syringe pack rather than the single syringe used across most of the range.

Lợi ích chính của Belotero Volume Lidocaine

  • The volumising grade of the range, placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, temples and chin and to treat severe nasolabial folds
  • Sodium hyaluronate 26 mg/ml with lidocaine hydrochloride 3.0 mg/ml, the most concentrated grade in the range
  • Cross-linked using 1,4-butanediol diglycidyl ether (BDDE) in a physiological phosphate buffer at pH 7
  • Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin
  • Contains lidocaine to reduce the sensation of pain and improve comfort during injection
  • Supplied as a 2 x 1 mL pack, a two-syringe unit rather than the single syringe used across most of the range
  • CE marked 0123
Thông tin chính
Thương hiệu BELOTERO
Nhà sản xuất Merz Aesthetics
Xuất xứ Switzerland
Chứng nhận CE marked 0123
Thành phần Sodium hyaluronate 26 mg/ml and lidocaine hydrochloride 3.0 mg/ml, in physiological phosphate buffer pH 7. The sodium hyaluronate is cross-linked using 1,4-butanediol diglycidyl ether (BDDE)
Dung tích / Kích thước 1 ml
Đóng gói 2 x 1 mL
Kích thước kim Each syringe is supplied with two sterile CE-marked single-use needles, 27G ½" and 30G ½"
Loại sử dụng For professional use: qualified practitioners and clinics only
Độ sâu tiêm Deep subcutaneous layers or above the periosteum (supraperiosteal), for enhancement of the cheeks, temples and chin and for severe nasolabial folds
Liệu trình / Thời gian Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Maximum 8 mL per session, with a recommended maximum of 8 mL in the cheeks, 6 mL in the temples, 4 mL in the nasolabial folds and 5 mL in the chin. Treatment may be renewed within a year without exceeding an annual dose of 16 mL, and sessions in the same area must be spaced at least 2 weeks apart

Chỉ định và sử dụng chuyên môn

Chỉ định chính

  • Enhancement of the cheeks
  • Enhancement of the temples
  • Enhancement of the chin
  • Treatment of severe nasolabial folds

Sử dụng chuyên môn

This product is designed to be injected only by authorised healthcare practitioners who have appropriate training and experience and who are qualified or accredited in accordance with national law. It is not for retail sale to consumers and not for self-application. Injection technique, plane, quantity and patient selection are determined by the treating practitioner, and the injection depth is specific to this grade and must not be inherited from another grade in the range.

Vùng điều trị

  • Cheeks
  • Temples
  • Chin
  • Nasolabial folds

Đối tượng bệnh nhân

Suitable for adult patients assessed as appropriate by the treating practitioner. The product is contraindicated in cases of known hypersensitivity to any of its components, especially sodium hyaluronate, lidocaine hydrochloride, BDDE or other amide-type local anaesthetics; in pregnant and breast-feeding women; in patients under 18 years old; in patients presenting a general infection; and in patients presenting an active auto-immune disease. It must not be injected into blood vessels, into areas presenting cutaneous inflammation or infection of immunological, allergic, bacterial, fungal or viral origin, into an area previously treated with a permanent dermal filler, or into the glabellar or nose region. It must not be used in association with other aesthetic techniques such as peeling, dermabrasion or laser treatment before complete healing of the last treatment, and in no case earlier than two weeks after it. Particular care applies to patients taking anticoagulant, antiplatelet, thrombolytic or anti-inflammatory medication, and to patients pre-disposed to hypertrophic scars or keloids. Patient selection and suitability are determined by the practitioner at consultation.

Cơ chế hoạt động của Belotero Volume Lidocaine ​

Belotero Volume Lidocaine works through sodium hyaluronate at 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), with lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7. As the volumising grade it acts as an injectable biodegradable implant placed in the deep subcutaneous layers or above the periosteum, which is why it is directed at the cheeks, temples and chin and at severe nasolabial folds rather than at fine lines. The lidocaine is included to reduce the sensation of pain and improve comfort during injection, and does not alter that mechanism.

Vì sao nên đặt hàng tại Allpara

Allpara cung cấp sản phẩm BELOTERO chính hãng, đã được xác minh, từ các nhà cung cấp được tuyển chọn, với khả năng truy xuất lô đầy đủ và hỗ trợ chuyên môn. Chúng tôi phục vụ các phòng khám và chuyên gia thẩm mỹ với sản phẩm đạt chứng nhận CE, giao hàng nhanh khắp EU từ kho tại EU và giá chuyên nghiệp cạnh tranh. Ưu tiên của chúng tôi là sự an toàn, hài lòng và kết quả của bệnh nhân của bạn, cùng dịch vụ hậu mãi tận tâm để bạn hoàn toàn yên tâm.

Câu hỏi thường gặp

Which BELOTERO grade is Belotero Volume Lidocaine?

Belotero Volume Lidocaine is the volumising grade, supplied at 26 mg/ml sodium hyaluronate with lidocaine hydrochloride 3.0 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE). At 26 mg/ml it is the most concentrated grade in the range and is placed in the deep subcutaneous layers or above the periosteum. Grades are not interchangeable.

Which treatment areas is Belotero Volume Lidocaine used for?

It is placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, the temples and the chin, or to treat severe nasolabial folds. Area selection and placement depth are the treating practitioner's decisions.

How long do the effects of Belotero Volume Lidocaine last?

Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Duration varies with the patient, the area treated, the volume placed and the injection technique.

Thêm sản phẩm từ Merz

Xem nhà sản xuất

BELOTERO mã hàng do ALLPARA lưu kho cho mục đích chuyên môn, nhập trực tiếp và có chứng nhận cho mỗi lô giao.

Xem BELOTERO sản phẩm

Lựa chọn thay thế cho phòng khám

Tất cả sản phẩm

Belotero Volume Lidocaine

Còn hàng
Đạt dấu CE Đạt dấu CE Belotero Volume Lidocaine
Giá chỉ dành cho tài khoản đã xác minh
Đăng nhập hoặc đăng ký tài khoản B2B để xem giá của bạn.
Đăng ký tài khoản B2B

Belotero Volume Lidocaine by Merz Aesthetics is the volumising grade of the BELOTERO range, a hyaluronic acid dermal filler supplied with lidocaine in the syringe and developed for severe nasolabial folds and to enhance the cheeks, the temples and the chin. Injection is into the deep subcutaneous layers or on top of the periosteum, with effects lasting up to 18 months in the nasolabial folds and up to 12 months in the cheeks, temples and chin. Each 1 mL contains sodium hyaluronate 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), and lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7, which makes it the most concentrated grade in the range. Belotero Volume filler is supplied as 2 x 1 mL, a two-syringe pack rather than the single syringe used across most of the range.

Lợi ích chính của Belotero Volume Lidocaine

  • The volumising grade of the range, placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, temples and chin and to treat severe nasolabial folds
  • Sodium hyaluronate 26 mg/ml with lidocaine hydrochloride 3.0 mg/ml, the most concentrated grade in the range
  • Cross-linked using 1,4-butanediol diglycidyl ether (BDDE) in a physiological phosphate buffer at pH 7
  • Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin
  • Contains lidocaine to reduce the sensation of pain and improve comfort during injection
  • Supplied as a 2 x 1 mL pack, a two-syringe unit rather than the single syringe used across most of the range
  • CE marked 0123
Thông tin chính
Thương hiệu BELOTERO
Nhà sản xuất Merz Aesthetics
Xuất xứ Switzerland
Chứng nhận CE marked 0123
Thành phần Sodium hyaluronate 26 mg/ml and lidocaine hydrochloride 3.0 mg/ml, in physiological phosphate buffer pH 7. The sodium hyaluronate is cross-linked using 1,4-butanediol diglycidyl ether (BDDE)
Dung tích / Kích thước 1 ml
Đóng gói 2 x 1 mL
Kích thước kim Each syringe is supplied with two sterile CE-marked single-use needles, 27G ½" and 30G ½"
Loại sử dụng For professional use: qualified practitioners and clinics only
Độ sâu tiêm Deep subcutaneous layers or above the periosteum (supraperiosteal), for enhancement of the cheeks, temples and chin and for severe nasolabial folds
Liệu trình / Thời gian Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Maximum 8 mL per session, with a recommended maximum of 8 mL in the cheeks, 6 mL in the temples, 4 mL in the nasolabial folds and 5 mL in the chin. Treatment may be renewed within a year without exceeding an annual dose of 16 mL, and sessions in the same area must be spaced at least 2 weeks apart

Chỉ định và sử dụng chuyên môn

Chỉ định chính

  • Enhancement of the cheeks
  • Enhancement of the temples
  • Enhancement of the chin
  • Treatment of severe nasolabial folds

Sử dụng chuyên môn

This product is designed to be injected only by authorised healthcare practitioners who have appropriate training and experience and who are qualified or accredited in accordance with national law. It is not for retail sale to consumers and not for self-application. Injection technique, plane, quantity and patient selection are determined by the treating practitioner, and the injection depth is specific to this grade and must not be inherited from another grade in the range.

Vùng điều trị

  • Cheeks
  • Temples
  • Chin
  • Nasolabial folds

Đối tượng bệnh nhân

Suitable for adult patients assessed as appropriate by the treating practitioner. The product is contraindicated in cases of known hypersensitivity to any of its components, especially sodium hyaluronate, lidocaine hydrochloride, BDDE or other amide-type local anaesthetics; in pregnant and breast-feeding women; in patients under 18 years old; in patients presenting a general infection; and in patients presenting an active auto-immune disease. It must not be injected into blood vessels, into areas presenting cutaneous inflammation or infection of immunological, allergic, bacterial, fungal or viral origin, into an area previously treated with a permanent dermal filler, or into the glabellar or nose region. It must not be used in association with other aesthetic techniques such as peeling, dermabrasion or laser treatment before complete healing of the last treatment, and in no case earlier than two weeks after it. Particular care applies to patients taking anticoagulant, antiplatelet, thrombolytic or anti-inflammatory medication, and to patients pre-disposed to hypertrophic scars or keloids. Patient selection and suitability are determined by the practitioner at consultation.

Cơ chế hoạt động của Belotero Volume Lidocaine ​

Belotero Volume Lidocaine works through sodium hyaluronate at 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), with lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7. As the volumising grade it acts as an injectable biodegradable implant placed in the deep subcutaneous layers or above the periosteum, which is why it is directed at the cheeks, temples and chin and at severe nasolabial folds rather than at fine lines. The lidocaine is included to reduce the sensation of pain and improve comfort during injection, and does not alter that mechanism.

Vì sao nên đặt hàng tại Allpara

Allpara cung cấp sản phẩm BELOTERO chính hãng, đã được xác minh, với khả năng truy xuất lô đầy đủ, hàng đạt chứng nhận CE, giao hàng nhanh khắp EU và hỗ trợ hậu mãi chuyên nghiệp.

Câu hỏi thường gặp

Which BELOTERO grade is Belotero Volume Lidocaine?

Belotero Volume Lidocaine is the volumising grade, supplied at 26 mg/ml sodium hyaluronate with lidocaine hydrochloride 3.0 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE). At 26 mg/ml it is the most concentrated grade in the range and is placed in the deep subcutaneous layers or above the periosteum. Grades are not interchangeable.

Which treatment areas is Belotero Volume Lidocaine used for?

It is placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, the temples and the chin, or to treat severe nasolabial folds. Area selection and placement depth are the treating practitioner's decisions.

How long do the effects of Belotero Volume Lidocaine last?

Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Duration varies with the patient, the area treated, the volume placed and the injection technique.

Thêm sản phẩm từ Merz

Xem nhà sản xuất →
* Sản phẩm dùng cho chuyên môn. Bao bì có thể khác nhau tùy theo lô hoặc thị trường. Vui lòng tham khảo hướng dẫn sử dụng kèm theo để biết đầy đủ cách dùng và chống chỉ định.