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SKU 11097

Restylane

Em stock
Volume
1x1mL
Laboratório
Galderma
Origem
Suécia
Indicação
Moderate to severe wrinkles and folds, lip augmentation
O preço profissional e o histórico são exclusivos de contas verificadas
allpara fornece profissionais licenciados. Inicie sessão ou peça uma conta B2B para ver os preços em tempo real, os escalões por volume e o histórico de preços.

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.

Principais vantagens de 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
Informação essencial
Marca RESTYLANE
Fabricante Galderma
País de origem Sweden
Certificação CE marked in accordance with Regulation (EU) 2017/745. The needles supplied are CE marked 0197
Composição 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
Volume / Tamanho 1 mL per syringe
Embalagem 1 x 1 mL glass syringe with luer-lock fitting and patient record label
Tamanho da agulha 30G x 1/2 inch or 29G x 1/2 inch, co-packed
Tipo de utilização For professional use. Injectable dermal filler
Profundidade de injeção Mid-to-deep dermal for wrinkles and folds; submucosal for lip augmentation
Protocolo / Duração 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

Indicações e utilização profissional

Principais indicações

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

Utilização profissional

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.

Zonas de tratamento

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

Perfil do paciente

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.

Como funciona 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.

Porquê encomendar na Allpara

A Allpara oferece produtos RESTYLANE originais e verificados de fornecedores selecionados, com rastreabilidade total dos lotes e apoio especializado. Servimos clínicas e profissionais de estética com produtos com certificação CE, entrega rápida em toda a UE a partir do nosso armazém na UE e preços profissionais competitivos. A nossa prioridade é a segurança, a satisfação e os resultados dos seus pacientes, com apoio pós-venda dedicado para a sua tranquilidade.

Perguntas frequentes

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.

Mais de Galderma

Ver laboratório

RESTYLANE referências disponíveis na ALLPARA para uso profissional, de origem direta e certificadas em cada envio.

Ver RESTYLANE produtos

RESTYLANE SKINBOOSTERS referências disponíveis na ALLPARA para uso profissional, de origem direta e certificadas em cada envio.

Ver RESTYLANE SKINBOOSTERS produtos

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Restylane

Em stock
Marcação CE Marcação CE Restylane
Preços exclusivos para contas verificadas
Inicie sessão ou peça uma conta B2B para ver o seu preço.
Pedir conta 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.

Principais vantagens de 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
Informação essencial
Marca RESTYLANE
Fabricante Galderma
País de origem Sweden
Certificação CE marked in accordance with Regulation (EU) 2017/745. The needles supplied are CE marked 0197
Composição 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
Volume / Tamanho 1 mL per syringe
Embalagem 1 x 1 mL glass syringe with luer-lock fitting and patient record label
Tamanho da agulha 30G x 1/2 inch or 29G x 1/2 inch, co-packed
Tipo de utilização For professional use. Injectable dermal filler
Profundidade de injeção Mid-to-deep dermal for wrinkles and folds; submucosal for lip augmentation
Protocolo / Duração 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

Indicações e utilização profissional

Principais indicações

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

Utilização profissional

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.

Zonas de tratamento

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

Perfil do paciente

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.

Como funciona 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.

Porquê encomendar na Allpara

A Allpara oferece produtos RESTYLANE originais e verificados, com rastreabilidade total dos lotes, stock com certificação CE, entrega rápida em toda a UE e apoio pós-venda especializado.

Perguntas frequentes

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.

Mais de Galderma

Ver o laboratório →
* Produto de uso profissional. A embalagem pode variar consoante o lote ou o mercado. Consulte as instruções de utilização fornecidas para as indicações completas e as contraindicações.