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SKU 11118

Revanesse Lips™+

In stock
Volume
2 x 1,2 mL
Laboratory
Prollenium Medical Technologies Inc.
Origin
カナダ
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Revanesse Lips+ is a biocompatible, biodegradable, non-pyrogenic, sterile, injectable viscoelastic hydrogel, clear and colourless, from Prollenium Medical Technologies in Aurora, Canada, developed for lip augmentation. It is indicated for submucosal implantation in patients 22 years of age or older and is FDA approved under PMA P160042/S010. The gel carries 25 mg/mL of bioresorbable, BDDE cross-linked hyaluronic acid, produced by the Streptococcus species of bacteria, with 0.3% lidocaine and is intended for professional use. A box holds two 1.2 mL glass syringes and two 0.5 inch 30-gauge sterile needles.

*Note: This product is FDA-approved in the United States. Regulatory status and availability may vary by country. Please contact ALLPARA to confirm availability for your market.

主なメリット: Revanesse Lips™+

  • BDDE cross-linked hyaluronic acid 25 mg/mL with 0.3% lidocaine
  • Indicated specifically for lip augmentation by submucosal implantation
  • FDA approved under PMA P160042/S010
  • Supplied with two 0.5 inch 30-gauge sterile needles
  • Supplied as two 1.2 mL glass syringes per box
  • Hyaluronic acid produced by the Streptococcus species of bacteria
  • Removable label portion for the patient record
主な情報
ブランド REVANESSE
製造元 Prollenium Medical Technologies Inc.
原産国 Canada
認証 FDA approved under PMA P160042/S010
成分 BDDE cross-linked hyaluronic acid 25 mg/mL with 0.3% lidocaine, in a bioresorbable, biocompatible, biodegradable, non-pyrogenic, sterile viscoelastic clear colourless hydrogel. The hyaluronic acid is produced by the Streptococcus species of bacteria.
容量 / サイズ 1.2 ml
包装 2 pre-filled glass syringes x 1.2 mL, with two 0.5 inch 30-gauge sterile needles. The syringe label carries a removable portion for the patient record.
針のサイズ 30G 1/2 inch, two supplied
使用タイプ For professional use: injectable dermal filler with lidocaine, for lip augmentation in patients 22 years of age or older
注入の深さ Submucosal implantation

適応と専門的な使用

主な適応

  • Lip augmentation by submucosal implantation

専門的な使用

For professional use. Revanesse Lips+ is administered by qualified physicians trained in the proper injection technique, and is not for retail sale or self-administration. It is placed by submucosal implantation in the lip using the 0.5 inch 30-gauge needles supplied. Its approval was supported by two clinical studies: a multicentre, double-blind, randomised, controlled treatment study enrolling 158 subjects over 10 months, and a multicentre, open-label retreatment study of 84 of those subjects over a further 8 months, with lip fullness assessed on the 5-point Lip Fullness Grading Scale.

施術部位

  • Lips

対象となる患者

Indicated for patients 22 years of age or older seeking lip augmentation. It must not be used in patients who develop hypertrophic scarring or keloid formation, in patients with evidence of scars at the intended treatment sites, in patients with acne or other inflammatory skin disease, in patients with multiple severe allergies or a history of allergy, or in patients with unattainable expectations. It must never be used in conjunction with laser, intense pulsed light, chemical peeling or dermabrasion treatments, or with over-the-counter or prescription wrinkle treatments within 4 weeks of treatment.

作用の仕組み: Revanesse Lips™+ ​

Lips+ is placed submucosally in the lip, where the cross-linked hyaluronic acid hydrogel adds volume directly. It is the only reference in the Revanesse range with an indication written specifically and solely for lip augmentation, which is reflected in its delivery: a fine 0.5 inch 30-gauge needle rather than the 27G used by the deeper-placed grades. The 0.3% lidocaine is present for injection comfort. Each syringe carries a removable portion of its label that can be affixed to the patient record for traceability.

Allparaで注文する理由

Allparaは、正規品で検証済みの REVANESSE 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 Revanesse Lips™+ differ from the other Revanesse references?

Its indication is written solely for lip augmentation, by submucosal implantation, in patients 22 years of age or older. It shares the 25 mg/mL BDDE cross-linked hyaluronic acid and 0.3% lidocaine of Revanesse Contour™+ and Revanesse Sculpt™+, but is supplied with finer 0.5 inch 30-gauge needles rather than 27G.

What clinical evidence supports Revanesse Lips+?

Two studies formed the basis of the PMA approval decision: a multicentre, double-blind, randomised, controlled treatment study of 158 subjects lasting 10 months, and a multicentre, open-label retreatment study of 84 of those subjects lasting a further 8 months. Effectiveness was measured as change in overall Lip Fullness Grading Scale score for both lips together.

その他の製品: Prollenium Medical Technologies

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Revanesse Lips™+

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Revanesse Lips+ is a biocompatible, biodegradable, non-pyrogenic, sterile, injectable viscoelastic hydrogel, clear and colourless, from Prollenium Medical Technologies in Aurora, Canada, developed for lip augmentation. It is indicated for submucosal implantation in patients 22 years of age or older and is FDA approved under PMA P160042/S010. The gel carries 25 mg/mL of bioresorbable, BDDE cross-linked hyaluronic acid, produced by the Streptococcus species of bacteria, with 0.3% lidocaine and is intended for professional use. A box holds two 1.2 mL glass syringes and two 0.5 inch 30-gauge sterile needles.

*Note: This product is FDA-approved in the United States. Regulatory status and availability may vary by country. Please contact ALLPARA to confirm availability for your market.

主なメリット: Revanesse Lips™+

  • BDDE cross-linked hyaluronic acid 25 mg/mL with 0.3% lidocaine
  • Indicated specifically for lip augmentation by submucosal implantation
  • FDA approved under PMA P160042/S010
  • Supplied with two 0.5 inch 30-gauge sterile needles
  • Supplied as two 1.2 mL glass syringes per box
  • Hyaluronic acid produced by the Streptococcus species of bacteria
  • Removable label portion for the patient record
主な情報
ブランド REVANESSE
製造元 Prollenium Medical Technologies Inc.
原産国 Canada
認証 FDA approved under PMA P160042/S010
成分 BDDE cross-linked hyaluronic acid 25 mg/mL with 0.3% lidocaine, in a bioresorbable, biocompatible, biodegradable, non-pyrogenic, sterile viscoelastic clear colourless hydrogel. The hyaluronic acid is produced by the Streptococcus species of bacteria.
容量 / サイズ 1.2 ml
包装 2 pre-filled glass syringes x 1.2 mL, with two 0.5 inch 30-gauge sterile needles. The syringe label carries a removable portion for the patient record.
針のサイズ 30G 1/2 inch, two supplied
使用タイプ For professional use: injectable dermal filler with lidocaine, for lip augmentation in patients 22 years of age or older
注入の深さ Submucosal implantation

適応と専門的な使用

主な適応

  • Lip augmentation by submucosal implantation

専門的な使用

For professional use. Revanesse Lips+ is administered by qualified physicians trained in the proper injection technique, and is not for retail sale or self-administration. It is placed by submucosal implantation in the lip using the 0.5 inch 30-gauge needles supplied. Its approval was supported by two clinical studies: a multicentre, double-blind, randomised, controlled treatment study enrolling 158 subjects over 10 months, and a multicentre, open-label retreatment study of 84 of those subjects over a further 8 months, with lip fullness assessed on the 5-point Lip Fullness Grading Scale.

施術部位

  • Lips

対象となる患者

Indicated for patients 22 years of age or older seeking lip augmentation. It must not be used in patients who develop hypertrophic scarring or keloid formation, in patients with evidence of scars at the intended treatment sites, in patients with acne or other inflammatory skin disease, in patients with multiple severe allergies or a history of allergy, or in patients with unattainable expectations. It must never be used in conjunction with laser, intense pulsed light, chemical peeling or dermabrasion treatments, or with over-the-counter or prescription wrinkle treatments within 4 weeks of treatment.

作用の仕組み: Revanesse Lips™+ ​

Lips+ is placed submucosally in the lip, where the cross-linked hyaluronic acid hydrogel adds volume directly. It is the only reference in the Revanesse range with an indication written specifically and solely for lip augmentation, which is reflected in its delivery: a fine 0.5 inch 30-gauge needle rather than the 27G used by the deeper-placed grades. The 0.3% lidocaine is present for injection comfort. Each syringe carries a removable portion of its label that can be affixed to the patient record for traceability.

Allparaで注文する理由

Allparaは、正規品で検証済みの REVANESSE 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 Revanesse Lips™+ differ from the other Revanesse references?

Its indication is written solely for lip augmentation, by submucosal implantation, in patients 22 years of age or older. It shares the 25 mg/mL BDDE cross-linked hyaluronic acid and 0.3% lidocaine of Revanesse Contour™+ and Revanesse Sculpt™+, but is supplied with finer 0.5 inch 30-gauge needles rather than 27G.

What clinical evidence supports Revanesse Lips+?

Two studies formed the basis of the PMA approval decision: a multicentre, double-blind, randomised, controlled treatment study of 158 subjects lasting 10 months, and a multicentre, open-label retreatment study of 84 of those subjects lasting a further 8 months. Effectiveness was measured as change in overall Lip Fullness Grading Scale score for both lips together.

その他の製品: Prollenium Medical Technologies

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