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SKU 11100

Restylane Eyelight Lidocaine

有货
容量
1 x 0,5 mL
制造商
Galderma
产地
瑞典
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allpara 仅向持证从业者供货。请登录或申请 B2B 账户,查看实时价格、批量阶梯价及价格历史。

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.

主要优势: 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
关键信息
品牌 RESTYLANE
制造商 Galderma
原产国 Sweden
认证 CE-marked
成分 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
容量 / 规格 0.5 ml
包装 1 x 0.5 mL prefilled syringe, co-packed with a sterilised needle and patient record labels
针头规格 29G x 1/2 inch. A blunt-tip cannula of 25G to 27G, 1.5 or 2 inches in length, may be used instead
使用类型 For professional use. Injectable under-eye filler
注射深度 Supraperiosteal, in the infraorbital hollow
方案 / 疗程 Maximum 1 ml per side per treatment session. If more than 1 ml per side is needed, a follow-up treatment session is recommended

适应症与专业用途

主要适应症

  • Improvement of infraorbital hollowing, by supraperiosteal placement

专业用途

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.

治疗部位

  • Infraorbital hollows, the under-eye area

适用患者

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.

作用原理: 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.

为什么选择在 Allpara 订购

Allpara 提供正品、经过验证的 RESTYLANE 产品,来自经过严格审核的供应商,具备完整的批次可追溯性和专家支持。我们为诊所和医美专业人士提供CE认证产品、从欧盟仓库快速配送至欧盟各地,以及具有竞争力的专业价格。我们关注的是您患者的安全、满意度和效果,并提供专属售后支持,让您安心无忧。

常见问题

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.

更多产品: Galderma

查看制造商

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Restylane Eyelight Lidocaine

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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.

主要优势: 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
关键信息
品牌 RESTYLANE
制造商 Galderma
原产国 Sweden
认证 CE-marked
成分 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
容量 / 规格 0.5 ml
包装 1 x 0.5 mL prefilled syringe, co-packed with a sterilised needle and patient record labels
针头规格 29G x 1/2 inch. A blunt-tip cannula of 25G to 27G, 1.5 or 2 inches in length, may be used instead
使用类型 For professional use. Injectable under-eye filler
注射深度 Supraperiosteal, in the infraorbital hollow
方案 / 疗程 Maximum 1 ml per side per treatment session. If more than 1 ml per side is needed, a follow-up treatment session is recommended

适应症与专业用途

主要适应症

  • Improvement of infraorbital hollowing, by supraperiosteal placement

专业用途

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.

治疗部位

  • Infraorbital hollows, the under-eye area

适用患者

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.

作用原理: 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.

为什么选择在 Allpara 订购

Allpara 提供正品、经过验证的 RESTYLANE 产品,具备完整的批次可追溯性、CE认证库存、欧盟范围内快速配送以及专业的售后支持。

常见问题

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.

更多产品: Galderma

查看制造商 →
* 专业用途产品。包装可能因批次或市场而异。完整的使用说明和禁忌症请参阅随附的使用说明书。