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SKU 11097

Restylane

Còn hàng
Dung tích
1x1mL
Nhà sản xuất
Galderma
Xuất xứ
Thụy Điển
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.

Restylane is a NASHA hyaluronic acid dermal filler, formulated to correct facial wrinkles and folds of moderate to severe depth at mid-to-deep dermal level. It is used on the nasolabial folds and for lip augmentation, and because it contains no anaesthetic it may be preferred where lidocaine is undesirable or contraindicated. The gel is stabilised hyaluronic acid cross-linked with BDDE and is supplied for professional use only.

Lợi ích chính của Restylane

  • Contains no lidocaine, so it can be used where an anaesthetic is undesirable or contraindicated
  • NASHA technology gives a stable gel structure that supports precise placement
  • Designed to integrate into dermal tissue while preserving facial expression and movement
  • Corrects moderate to severe wrinkles and folds through volumisation and hydration
  • Covers both facial folds and lip augmentation from a single reference
  • Hyaluronic acid based, so the implant can be broken down by enzymatic degradation with hyaluronidase where clinically indicated
  • Duration of effectiveness of 18 months in the nasolabial folds following re-treatment at 4.5 or 9 months
  • Supplied with sterilised needles, either 30G x 1/2 inch or 29G x 1/2 inch
Thông tin chính
Thương hiệu RESTYLANE
Nhà sản xuất Galderma
Xuất xứ Sweden
Chứng nhận CE marked in accordance with Regulation (EU) 2017/745. The needles supplied are CE marked 0197
Thành phần Gel of hyaluronic acid generated by Streptococcus species of bacteria, chemically cross-linked with 1,4-butanediol diglycidyl ether (BDDE), stabilised and suspended in phosphate-buffered saline at pH 7. Hyaluronic acid 20 mg/mL. Contains no lidocaine
Dung tích / Kích thước 1 mL per syringe
Đóng gói 1 x 1 mL glass syringe with luer-lock fitting and patient record label
Kích thước kim 30G x 1/2 inch or 29G x 1/2 inch, co-packed
Loại sử dụng For professional use. Injectable dermal filler
Độ sâu tiêm Mid-to-deep dermal for wrinkles and folds; submucosal for lip augmentation
Liệu trình / Thời gian Duration of effectiveness of 18 months from baseline in the nasolabial folds, following re-treatment at 4.5 or 9 months. Maximum 6 ml per patient per treatment in wrinkles and folds such as the nasolabial folds, and 1.5 ml per lip per treatment

Chỉ định và sử dụng chuyên môn

Chỉ định chính

  • Moderate to severe facial wrinkles and folds, such as nasolabial folds, by mid-to-deep dermal implantation
  • Lip augmentation by submucosal implantation

Sử dụng chuyên môn

Restylane is an injectable medical device for administration only by licensed, appropriately trained healthcare practitioners in a controlled clinical setting, and is not for retail sale or self-administration. It is indicated for mid-to-deep dermal implantation for wrinkles and folds and for submucosal implantation for lip augmentation, and is contraindicated for implantation in anatomical spaces other than these. It must not be implanted into blood vessels and should not be used in vascular rich areas, since localised superficial necrosis and scarring may occur after injection in or near vessels.

Vùng điều trị

  • Nasolabial folds
  • Moderate to severe facial wrinkles and folds
  • Lips, for augmentation

Đối tượng bệnh nhân

For adult patients assessed as suitable by the treating practitioner. Patient selection, treatment area, injected volume and injection plane are determined by the practitioner following clinical assessment. Because this reference contains no lidocaine, it is the appropriate choice where an amide-type local anaesthetic is contraindicated or where the practitioner prefers to control anaesthesia separately. It is contraindicated in patients with severe allergies manifested by a history of anaphylaxis, or a history or presence of multiple severe allergies, in patients with a history of allergy to gram-positive bacterial proteins, since the gel contains trace amounts of such material, and in patients with bleeding disorders. Use should be deferred at sites where an active inflammatory process such as cysts, pimples, rashes or hives, or an infection, is present until that process has been controlled.

Cơ chế hoạt động của Restylane ​

Restylane works through non-animal stabilised hyaluronic acid produced by fermentation and cross-linked with BDDE, which binds water and restores volume when implanted in the mid to deep dermis. The NASHA structure holds its form rather than spreading, so the gel integrates into dermal tissue while allowing normal facial movement. This makes it suitable for practitioners correcting moderate to severe folds who need predictable placement and no incorporated anaesthetic.

Vì sao nên đặt hàng tại Allpara

Allpara cung cấp sản phẩm RESTYLANE 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

How does Restylane differ from Restylane Lidocaine?

Both carry the same hyaluronic acid concentration of 20 mg/mL and both are cross-linked with BDDE. The difference is the anaesthetic: Restylane Lidocaine contains lidocaine hydrochloride 3 mg/mL, while Restylane contains none. Restylane is therefore the reference to use where lidocaine is undesirable or contraindicated, and the two are not interchangeable in that situation.

Which technology does Restylane use?

Restylane uses NASHA, non-animal stabilised hyaluronic acid generated by Streptococcus species of bacteria and cross-linked with 1,4-butanediol diglycidyl ether. The gel is suspended in phosphate-buffered saline at pH 7. The stabilised structure is what supports precise placement and integration into dermal tissue.

Thêm sản phẩm từ Galderma

Xem nhà sản xuất

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

Xem RESTYLANE sản phẩm

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

Xem RESTYLANE SKINBOOSTERS sản phẩm

Lựa chọn thay thế cho phòng khám

Tất cả sản phẩm

Restylane

Còn hàng
Đạt dấu CE Đạt dấu CE Restylane
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

Restylane is a NASHA hyaluronic acid dermal filler, formulated to correct facial wrinkles and folds of moderate to severe depth at mid-to-deep dermal level. It is used on the nasolabial folds and for lip augmentation, and because it contains no anaesthetic it may be preferred where lidocaine is undesirable or contraindicated. The gel is stabilised hyaluronic acid cross-linked with BDDE and is supplied for professional use only.

Lợi ích chính của Restylane

  • Contains no lidocaine, so it can be used where an anaesthetic is undesirable or contraindicated
  • NASHA technology gives a stable gel structure that supports precise placement
  • Designed to integrate into dermal tissue while preserving facial expression and movement
  • Corrects moderate to severe wrinkles and folds through volumisation and hydration
  • Covers both facial folds and lip augmentation from a single reference
  • Hyaluronic acid based, so the implant can be broken down by enzymatic degradation with hyaluronidase where clinically indicated
  • Duration of effectiveness of 18 months in the nasolabial folds following re-treatment at 4.5 or 9 months
  • Supplied with sterilised needles, either 30G x 1/2 inch or 29G x 1/2 inch
Thông tin chính
Thương hiệu RESTYLANE
Nhà sản xuất Galderma
Xuất xứ Sweden
Chứng nhận CE marked in accordance with Regulation (EU) 2017/745. The needles supplied are CE marked 0197
Thành phần Gel of hyaluronic acid generated by Streptococcus species of bacteria, chemically cross-linked with 1,4-butanediol diglycidyl ether (BDDE), stabilised and suspended in phosphate-buffered saline at pH 7. Hyaluronic acid 20 mg/mL. Contains no lidocaine
Dung tích / Kích thước 1 mL per syringe
Đóng gói 1 x 1 mL glass syringe with luer-lock fitting and patient record label
Kích thước kim 30G x 1/2 inch or 29G x 1/2 inch, co-packed
Loại sử dụng For professional use. Injectable dermal filler
Độ sâu tiêm Mid-to-deep dermal for wrinkles and folds; submucosal for lip augmentation
Liệu trình / Thời gian Duration of effectiveness of 18 months from baseline in the nasolabial folds, following re-treatment at 4.5 or 9 months. Maximum 6 ml per patient per treatment in wrinkles and folds such as the nasolabial folds, and 1.5 ml per lip per treatment

Chỉ định và sử dụng chuyên môn

Chỉ định chính

  • Moderate to severe facial wrinkles and folds, such as nasolabial folds, by mid-to-deep dermal implantation
  • Lip augmentation by submucosal implantation

Sử dụng chuyên môn

Restylane is an injectable medical device for administration only by licensed, appropriately trained healthcare practitioners in a controlled clinical setting, and is not for retail sale or self-administration. It is indicated for mid-to-deep dermal implantation for wrinkles and folds and for submucosal implantation for lip augmentation, and is contraindicated for implantation in anatomical spaces other than these. It must not be implanted into blood vessels and should not be used in vascular rich areas, since localised superficial necrosis and scarring may occur after injection in or near vessels.

Vùng điều trị

  • Nasolabial folds
  • Moderate to severe facial wrinkles and folds
  • Lips, for augmentation

Đối tượng bệnh nhân

For adult patients assessed as suitable by the treating practitioner. Patient selection, treatment area, injected volume and injection plane are determined by the practitioner following clinical assessment. Because this reference contains no lidocaine, it is the appropriate choice where an amide-type local anaesthetic is contraindicated or where the practitioner prefers to control anaesthesia separately. It is contraindicated in patients with severe allergies manifested by a history of anaphylaxis, or a history or presence of multiple severe allergies, in patients with a history of allergy to gram-positive bacterial proteins, since the gel contains trace amounts of such material, and in patients with bleeding disorders. Use should be deferred at sites where an active inflammatory process such as cysts, pimples, rashes or hives, or an infection, is present until that process has been controlled.

Cơ chế hoạt động của Restylane ​

Restylane works through non-animal stabilised hyaluronic acid produced by fermentation and cross-linked with BDDE, which binds water and restores volume when implanted in the mid to deep dermis. The NASHA structure holds its form rather than spreading, so the gel integrates into dermal tissue while allowing normal facial movement. This makes it suitable for practitioners correcting moderate to severe folds who need predictable placement and no incorporated anaesthetic.

Vì sao nên đặt hàng tại Allpara

Allpara cung cấp sản phẩm RESTYLANE 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

How does Restylane differ from Restylane Lidocaine?

Both carry the same hyaluronic acid concentration of 20 mg/mL and both are cross-linked with BDDE. The difference is the anaesthetic: Restylane Lidocaine contains lidocaine hydrochloride 3 mg/mL, while Restylane contains none. Restylane is therefore the reference to use where lidocaine is undesirable or contraindicated, and the two are not interchangeable in that situation.

Which technology does Restylane use?

Restylane uses NASHA, non-animal stabilised hyaluronic acid generated by Streptococcus species of bacteria and cross-linked with 1,4-butanediol diglycidyl ether. The gel is suspended in phosphate-buffered saline at pH 7. The stabilised structure is what supports precise placement and integration into dermal tissue.

Thêm sản phẩm từ Galderma

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.