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SKU 10091

Belotero Soft Lidocaine

Em stock
Volume
1x1mL
Laboratório
Merz Aesthetics
Origem
Suíça
Indicação
Lines, folds and volume correction
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.

Belotero Soft Lidocaine by Merz Aesthetics is a biodegradable injectable implant, sterile, non-pyrogenic and viscoelastic, a colourless and transparent cross-linked sodium hyaluronate filler of non-animal origin, intended for filling perioral fine lines. It is placed in the superficial to mid-dermis and is designed to be injected by authorised practitioners with appropriate training and experience. Each 1 mL syringe contains 20.0 mg/ml of cross-linked sodium hyaluronate produced by fermentation of Streptococcus equi and 3.0 mg/ml (0.3%) lidocaine hydrochloride, in a physiological phosphate buffer at pH 7. The lidocaine is added to reduce local pain associated with injection and to improve patient comfort.

Principais vantagens de Belotero Soft Lidocaine

  • Injectable biodegradable implant indicated for filling of perioral fine lines
  • Cross-linked sodium hyaluronate 20.0 mg/ml with lidocaine hydrochloride 3.0 mg/ml, in phosphate buffer at pH 7
  • Indicated for injection into the superficial to mid-dermis, the lightest grade in the range
  • Contains 0.3% lidocaine hydrochloride to reduce local pain during injection and improve patient comfort
  • Sterile, non-pyrogenic, viscoelastic, colourless and transparent, and of non-animal origin
  • Hyaluronate produced by fermentation of Streptococcus equi rather than from an animal source
  • Supplied as one 1 mL syringe with two sterile CE-marked single-use needles and two traceability labels
Informação essencial
Marca BELOTERO
Fabricante Merz Aesthetics
País de origem Switzerland
Certificação CE marked in accordance with Directive 93/42/EEC relating to medical devices
Composição Cross-linked sodium hyaluronate 20.0 mg/ml and lidocaine hydrochloride 3.0 mg/ml, in phosphate buffer pH 7. The sodium hyaluronate is produced by fermentation of Streptococcus equi
Volume / Tamanho 1 ml
Embalagem 1 x 1 mL
Tamanho da agulha Two sterile CE-marked single-use 30G ½" needles supplied in the box
Tipo de utilização For professional use - qualified practitioners and clinics only
Profundidade de injeção Superficial to mid-dermis for perioral fine lines

Indicações e utilização profissional

Principais indicações

  • Filling of perioral fine lines
  • Injection into the superficial to mid-dermis

Utilização profissional

This product is designed to be injected only by authorised healthcare practitioners who have appropriate training and experience and who are qualified or accredited in accordance with national law. It is not for retail sale to consumers and not for self-application. Injection technique, plane, quantity and patient selection are determined by the treating practitioner, and the injection depth is specific to this grade and must not be inherited from another grade in the range.

Zonas de tratamento

  • Perioral fine lines

Perfil do paciente

Suitable for adult patients assessed as appropriate by the treating practitioner. The product is contra-indicated in cases of known hypersensitivity to any of its components, especially sodium hyaluronate, lidocaine hydrochloride, BDDE or other amide-type local anaesthetics; in pregnant and breast-feeding women; in patients under 18 years old; in patients presenting a general infection; and in patients presenting an active auto-immune disease. It must not be injected into blood vessels, into areas presenting cutaneous inflammation or infection of immunological, allergic, bacterial, fungal or viral origin, into an area previously treated with a permanent dermal filler, or into the glabellar or nose region. It must not be used in association with other aesthetic techniques such as peeling, dermabrasion or laser treatment before complete healing of the last treatment, and in no case earlier than two weeks after it. Particular care applies to patients taking anticoagulant, antiplatelet, thrombolytic or anti-inflammatory medication, and to patients pre-disposed to hypertrophic scars or keloids. Patient selection and suitability are determined by the practitioner at consultation.

Como funciona Belotero Soft Lidocaine ​

Belotero Soft Lidocaine works through cross-linked sodium hyaluronate, supplied at 20.0 mg/ml with lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7, made up to 1 mL. The gel is sterile, non-pyrogenic, viscoelastic, colourless, transparent and of non-animal origin, and acts as an injectable biodegradable implant that increases cutaneous tissue volume where it is placed. Placement is what defines this grade: it goes into the superficial to mid-dermis for the treatment of perioral fine lines. The lidocaine acts locally during administration to reduce pain associated with injection of the gel and does not alter that mechanism.

Porquê encomendar na Allpara

A Allpara oferece produtos BELOTERO 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

Which BELOTERO grade is Belotero Soft Lidocaine?

Belotero Soft Lidocaine is supplied at 20.0 mg/ml cross-linked sodium hyaluronate with lidocaine hydrochloride 3.0 mg/ml, and is placed in the superficial to mid-dermis for perioral fine lines. It is the lightest grade in the range. Belotero Balance Lidocaine is 22.5 mg/ml and covers a wider set of areas, and the two are not interchangeable.

Which treatment areas is Belotero Soft Lidocaine used for?

It is used in the superficial to mid-dermis for the treatment of perioral fine lines. Area selection and placement depth are the treating practitioner's decisions.

Mais de Merz

Ver laboratório

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

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Belotero Soft Lidocaine

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

Belotero Soft Lidocaine by Merz Aesthetics is a biodegradable injectable implant, sterile, non-pyrogenic and viscoelastic, a colourless and transparent cross-linked sodium hyaluronate filler of non-animal origin, intended for filling perioral fine lines. It is placed in the superficial to mid-dermis and is designed to be injected by authorised practitioners with appropriate training and experience. Each 1 mL syringe contains 20.0 mg/ml of cross-linked sodium hyaluronate produced by fermentation of Streptococcus equi and 3.0 mg/ml (0.3%) lidocaine hydrochloride, in a physiological phosphate buffer at pH 7. The lidocaine is added to reduce local pain associated with injection and to improve patient comfort.

Principais vantagens de Belotero Soft Lidocaine

  • Injectable biodegradable implant indicated for filling of perioral fine lines
  • Cross-linked sodium hyaluronate 20.0 mg/ml with lidocaine hydrochloride 3.0 mg/ml, in phosphate buffer at pH 7
  • Indicated for injection into the superficial to mid-dermis, the lightest grade in the range
  • Contains 0.3% lidocaine hydrochloride to reduce local pain during injection and improve patient comfort
  • Sterile, non-pyrogenic, viscoelastic, colourless and transparent, and of non-animal origin
  • Hyaluronate produced by fermentation of Streptococcus equi rather than from an animal source
  • Supplied as one 1 mL syringe with two sterile CE-marked single-use needles and two traceability labels
Informação essencial
Marca BELOTERO
Fabricante Merz Aesthetics
País de origem Switzerland
Certificação CE marked in accordance with Directive 93/42/EEC relating to medical devices
Composição Cross-linked sodium hyaluronate 20.0 mg/ml and lidocaine hydrochloride 3.0 mg/ml, in phosphate buffer pH 7. The sodium hyaluronate is produced by fermentation of Streptococcus equi
Volume / Tamanho 1 ml
Embalagem 1 x 1 mL
Tamanho da agulha Two sterile CE-marked single-use 30G ½" needles supplied in the box
Tipo de utilização For professional use - qualified practitioners and clinics only
Profundidade de injeção Superficial to mid-dermis for perioral fine lines

Indicações e utilização profissional

Principais indicações

  • Filling of perioral fine lines
  • Injection into the superficial to mid-dermis

Utilização profissional

This product is designed to be injected only by authorised healthcare practitioners who have appropriate training and experience and who are qualified or accredited in accordance with national law. It is not for retail sale to consumers and not for self-application. Injection technique, plane, quantity and patient selection are determined by the treating practitioner, and the injection depth is specific to this grade and must not be inherited from another grade in the range.

Zonas de tratamento

  • Perioral fine lines

Perfil do paciente

Suitable for adult patients assessed as appropriate by the treating practitioner. The product is contra-indicated in cases of known hypersensitivity to any of its components, especially sodium hyaluronate, lidocaine hydrochloride, BDDE or other amide-type local anaesthetics; in pregnant and breast-feeding women; in patients under 18 years old; in patients presenting a general infection; and in patients presenting an active auto-immune disease. It must not be injected into blood vessels, into areas presenting cutaneous inflammation or infection of immunological, allergic, bacterial, fungal or viral origin, into an area previously treated with a permanent dermal filler, or into the glabellar or nose region. It must not be used in association with other aesthetic techniques such as peeling, dermabrasion or laser treatment before complete healing of the last treatment, and in no case earlier than two weeks after it. Particular care applies to patients taking anticoagulant, antiplatelet, thrombolytic or anti-inflammatory medication, and to patients pre-disposed to hypertrophic scars or keloids. Patient selection and suitability are determined by the practitioner at consultation.

Como funciona Belotero Soft Lidocaine ​

Belotero Soft Lidocaine works through cross-linked sodium hyaluronate, supplied at 20.0 mg/ml with lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7, made up to 1 mL. The gel is sterile, non-pyrogenic, viscoelastic, colourless, transparent and of non-animal origin, and acts as an injectable biodegradable implant that increases cutaneous tissue volume where it is placed. Placement is what defines this grade: it goes into the superficial to mid-dermis for the treatment of perioral fine lines. The lidocaine acts locally during administration to reduce pain associated with injection of the gel and does not alter that mechanism.

Porquê encomendar na Allpara

A Allpara oferece produtos BELOTERO 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

Which BELOTERO grade is Belotero Soft Lidocaine?

Belotero Soft Lidocaine is supplied at 20.0 mg/ml cross-linked sodium hyaluronate with lidocaine hydrochloride 3.0 mg/ml, and is placed in the superficial to mid-dermis for perioral fine lines. It is the lightest grade in the range. Belotero Balance Lidocaine is 22.5 mg/ml and covers a wider set of areas, and the two are not interchangeable.

Which treatment areas is Belotero Soft Lidocaine used for?

It is used in the superficial to mid-dermis for the treatment of perioral fine lines. Area selection and placement depth are the treating practitioner's decisions.

Mais de Merz

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.