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SKU 11097

Restylane

In stock
Volume
1x1mL
Laboratory
Galderma
Origin
スウェーデン
Trade price and history are verified-only
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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.

主なメリット: 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
主な情報
ブランド RESTYLANE
製造元 Galderma
原産国 Sweden
認証 CE marked in accordance with Regulation (EU) 2017/745. The needles supplied are CE marked 0197
成分 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
容量 / サイズ 1 mL per syringe
包装 1 x 1 mL glass syringe with luer-lock fitting and patient record label
針のサイズ 30G x 1/2 inch or 29G x 1/2 inch, co-packed
使用タイプ For professional use. Injectable dermal filler
注入の深さ Mid-to-deep dermal for wrinkles and folds; submucosal for lip augmentation
プロトコル / 期間 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

適応と専門的な使用

主な適応

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

専門的な使用

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.

施術部位

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

対象となる患者

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.

作用の仕組み: 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.

Allparaで注文する理由

Allparaは、正規品で検証済みの RESTYLANE 製品を厳選されたサプライヤーから提供し、完全なロットトレーサビリティと専門家によるサポートを備えています。CE認証製品、EU倉庫からのEU全域への迅速な配送、競争力のある業務用価格で、クリニックと美容医療の専門家にサービスを提供しています。私たちが重視するのは患者様の安全、満足、そして結果です。安心してご利用いただけるよう、専任のアフターサポートをご用意しています。

よくある質問

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.

その他の製品: Galderma

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RESTYLANE references stocked by ALLPARA for professional use, sourced direct and certified on every shipment.

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RESTYLANE SKINBOOSTERS references stocked by ALLPARA for professional use, sourced direct and certified on every shipment.

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Restylane

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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.

主なメリット: 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
主な情報
ブランド RESTYLANE
製造元 Galderma
原産国 Sweden
認証 CE marked in accordance with Regulation (EU) 2017/745. The needles supplied are CE marked 0197
成分 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
容量 / サイズ 1 mL per syringe
包装 1 x 1 mL glass syringe with luer-lock fitting and patient record label
針のサイズ 30G x 1/2 inch or 29G x 1/2 inch, co-packed
使用タイプ For professional use. Injectable dermal filler
注入の深さ Mid-to-deep dermal for wrinkles and folds; submucosal for lip augmentation
プロトコル / 期間 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

適応と専門的な使用

主な適応

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

専門的な使用

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.

施術部位

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

対象となる患者

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.

作用の仕組み: 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.

Allparaで注文する理由

Allparaは、正規品で検証済みの RESTYLANE 製品を、完全なロットトレーサビリティ、CE認証在庫、EU全域への迅速な配送、専門的なアフターサポートとともに提供しています。

よくある質問

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.

その他の製品: Galderma

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* Professional-use product. Packaging may vary by batch or market. Refer to the supplied IFU for full directions and contraindications.