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SKU 11100

Restylane Eyelight Lidocaine

Còn hàng
Dung tích
1 x 0,5 mL
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 Eyelight Lidocaine is an under-eye hyaluronic acid filler, formulated specifically for infraorbital hollowing. The transparent, viscous gel contains hyaluronic acid at 20 mg/mL with 0.3% lidocaine hydrochloride and is supplied for professional use only.

Lợi ích chính của Restylane Eyelight Lidocaine

  • Formulated specifically for the delicate under-eye area rather than adapted from a facial filler
  • Indicated for the improvement of infraorbital hollowing
  • Supplied in a 0.5 mL syringe, which matches the small volumes tear-trough work requires and reduces waste per case
  • Transparent, viscous, sterile gel intended for natural-looking correction in thin periorbital skin
  • Contains lidocaine hydrochloride 3 mg/mL, relevant in an area patients find highly sensitive
  • Hyaluronic acid based, so the implant can be broken down by enzymatic degradation with hyaluronidase where clinically indicated
  • Placed supraperiosteally with a 29G x 1/2 inch needle, or with a 25G to 27G blunt-tip cannula
Thông tin chính
Thương hiệu RESTYLANE
Nhà sản xuất Galderma
Xuất xứ Sweden
Chứng nhận CE-marked
Thành phần Transparent, viscous, sterile gel of hyaluronic acid generated by Streptococcus species of bacteria, chemically cross-linked with 1,4-butanediol diglycidyl ether (BDDE), suspended in phosphate-buffered saline at pH 7. Hyaluronic acid 20 mg/mL with lidocaine hydrochloride 3 mg/mL
Dung tích / Kích thước 0.5 ml
Đóng gói 1 x 0.5 mL prefilled syringe, co-packed with a sterilised needle and patient record labels
Kích thước kim 29G x 1/2 inch. A blunt-tip cannula of 25G to 27G, 1.5 or 2 inches in length, may be used instead
Loại sử dụng For professional use. Injectable under-eye filler
Độ sâu tiêm Supraperiosteal, in the infraorbital hollow
Liệu trình / Thời gian Maximum 1 ml per side per treatment session. If more than 1 ml per side is needed, a follow-up treatment session is recommended

Chỉ định và sử dụng chuyên môn

Chỉ định chính

  • Improvement of infraorbital hollowing, by supraperiosteal placement

Sử dụng chuyên môn

Restylane Eyelight Lidocaine 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. Periorbital treatment is a technically demanding injectable procedure: the skin is thin, the anatomy is unforgiving, and complications are immediately visible, so it should be undertaken only by practitioners with specific training in the region. Injections into the infraorbital hollows are supraperiosteal, using a 29G x 1/2 inch needle or a blunt-tip cannula of 25G to 27G. Patients should be limited to up to 1 ml per side per treatment session; if more than 1 ml per side is needed to achieve optimal correction, a follow-up treatment session is recommended. Introduction into the vasculature may lead to embolisation, occlusion of the vessels, ischaemia or infarction, with rare reports of temporary or permanent vision impairment and blindness, so the product must be injected slowly with the least pressure necessary.

Vùng điều trị

  • Infraorbital hollows, the under-eye area

Đối tượng bệnh nhân

For patients assessed as suitable by the treating practitioner. Patient selection is particularly important in this region: skin thickness, fluid retention, existing pigmentation and the presence of fat herniation all affect whether filler is the appropriate answer to under-eye shadowing, and that assessment rests with the practitioner. Because the gel contains lidocaine hydrochloride 3 mg/mL, patients with known hypersensitivity to lidocaine or to other amide-type anaesthetics must not receive it. It is contraindicated in patients with severe allergies manifested by a history of anaphylaxis, or a history or presence of multiple severe allergies, and in patients with a history of allergy to gram-positive bacterial proteins, since the gel contains trace amounts of such material. Use should be deferred at sites where an active inflammatory process or infection is present until that process has been controlled.

Cơ chế hoạt động của Restylane Eyelight Lidocaine ​

Restylane Eyelight Lidocaine works through a smooth hyaluronic acid gel placed beneath the thin skin of the infraorbital region, where it restores lost volume so that the hollow no longer casts a shadow. The formulation is intended to give subtle correction rather than projection, because in periorbital skin even a small excess or an uneven plane is visible. The incorporated lidocaine hydrochloride reduces discomfort during injection only.

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

Can Restylane Eyelight Lidocaine be injected with a cannula?

Yes. It is administered with a thin gauge 29G x 1/2 inch needle or a blunt cannula of 25G to 27G with a length of 1.5 or 2 inches. Cannula injection has been clinically evaluated in one brand of blunt-tip cannula only.

Why does under-eye treatment require particular caution?

The periorbital skin is thin, the underlying anatomy is unforgiving and any irregularity or excess volume is immediately visible. Introduction of filler into the vasculature can cause embolisation, occlusion, ischaemia or infarction, and rare cases of temporary or permanent vision impairment and blindness have been reported after facial filler injection. For those reasons treatment should be undertaken only by practitioners with specific training in the area.

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 Eyelight Lidocaine

Còn hàng
Đạt dấu CE Đạt dấu CE Restylane Eyelight 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

Restylane Eyelight Lidocaine is an under-eye hyaluronic acid filler, formulated specifically for infraorbital hollowing. The transparent, viscous gel contains hyaluronic acid at 20 mg/mL with 0.3% lidocaine hydrochloride and is supplied for professional use only.

Lợi ích chính của Restylane Eyelight Lidocaine

  • Formulated specifically for the delicate under-eye area rather than adapted from a facial filler
  • Indicated for the improvement of infraorbital hollowing
  • Supplied in a 0.5 mL syringe, which matches the small volumes tear-trough work requires and reduces waste per case
  • Transparent, viscous, sterile gel intended for natural-looking correction in thin periorbital skin
  • Contains lidocaine hydrochloride 3 mg/mL, relevant in an area patients find highly sensitive
  • Hyaluronic acid based, so the implant can be broken down by enzymatic degradation with hyaluronidase where clinically indicated
  • Placed supraperiosteally with a 29G x 1/2 inch needle, or with a 25G to 27G blunt-tip cannula
Thông tin chính
Thương hiệu RESTYLANE
Nhà sản xuất Galderma
Xuất xứ Sweden
Chứng nhận CE-marked
Thành phần Transparent, viscous, sterile gel of hyaluronic acid generated by Streptococcus species of bacteria, chemically cross-linked with 1,4-butanediol diglycidyl ether (BDDE), suspended in phosphate-buffered saline at pH 7. Hyaluronic acid 20 mg/mL with lidocaine hydrochloride 3 mg/mL
Dung tích / Kích thước 0.5 ml
Đóng gói 1 x 0.5 mL prefilled syringe, co-packed with a sterilised needle and patient record labels
Kích thước kim 29G x 1/2 inch. A blunt-tip cannula of 25G to 27G, 1.5 or 2 inches in length, may be used instead
Loại sử dụng For professional use. Injectable under-eye filler
Độ sâu tiêm Supraperiosteal, in the infraorbital hollow
Liệu trình / Thời gian Maximum 1 ml per side per treatment session. If more than 1 ml per side is needed, a follow-up treatment session is recommended

Chỉ định và sử dụng chuyên môn

Chỉ định chính

  • Improvement of infraorbital hollowing, by supraperiosteal placement

Sử dụng chuyên môn

Restylane Eyelight Lidocaine 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. Periorbital treatment is a technically demanding injectable procedure: the skin is thin, the anatomy is unforgiving, and complications are immediately visible, so it should be undertaken only by practitioners with specific training in the region. Injections into the infraorbital hollows are supraperiosteal, using a 29G x 1/2 inch needle or a blunt-tip cannula of 25G to 27G. Patients should be limited to up to 1 ml per side per treatment session; if more than 1 ml per side is needed to achieve optimal correction, a follow-up treatment session is recommended. Introduction into the vasculature may lead to embolisation, occlusion of the vessels, ischaemia or infarction, with rare reports of temporary or permanent vision impairment and blindness, so the product must be injected slowly with the least pressure necessary.

Vùng điều trị

  • Infraorbital hollows, the under-eye area

Đối tượng bệnh nhân

For patients assessed as suitable by the treating practitioner. Patient selection is particularly important in this region: skin thickness, fluid retention, existing pigmentation and the presence of fat herniation all affect whether filler is the appropriate answer to under-eye shadowing, and that assessment rests with the practitioner. Because the gel contains lidocaine hydrochloride 3 mg/mL, patients with known hypersensitivity to lidocaine or to other amide-type anaesthetics must not receive it. It is contraindicated in patients with severe allergies manifested by a history of anaphylaxis, or a history or presence of multiple severe allergies, and in patients with a history of allergy to gram-positive bacterial proteins, since the gel contains trace amounts of such material. Use should be deferred at sites where an active inflammatory process or infection is present until that process has been controlled.

Cơ chế hoạt động của Restylane Eyelight Lidocaine ​

Restylane Eyelight Lidocaine works through a smooth hyaluronic acid gel placed beneath the thin skin of the infraorbital region, where it restores lost volume so that the hollow no longer casts a shadow. The formulation is intended to give subtle correction rather than projection, because in periorbital skin even a small excess or an uneven plane is visible. The incorporated lidocaine hydrochloride reduces discomfort during injection only.

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

Can Restylane Eyelight Lidocaine be injected with a cannula?

Yes. It is administered with a thin gauge 29G x 1/2 inch needle or a blunt cannula of 25G to 27G with a length of 1.5 or 2 inches. Cannula injection has been clinically evaluated in one brand of blunt-tip cannula only.

Why does under-eye treatment require particular caution?

The periorbital skin is thin, the underlying anatomy is unforgiving and any irregularity or excess volume is immediately visible. Introduction of filler into the vasculature can cause embolisation, occlusion, ischaemia or infarction, and rare cases of temporary or permanent vision impairment and blindness have been reported after facial filler injection. For those reasons treatment should be undertaken only by practitioners with specific training in the area.

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.