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· Rellenos dérmicos
SKU 10091

Belotero Soft Lidocaine

En stock
Volumen
1x1mL
Laboratorio
Merz Aesthetics
Origen
Suiza
Indicación
Lines, folds and volume correction
El precio profesional y su historial son solo para cuentas verificadas
allpara suministra a profesionales autorizados. Inicie sesión o solicite una cuenta B2B para ver los precios en tiempo real, los tramos por volumen y el historial de precios.

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.

Principales ventajas 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
Información clave
Marca BELOTERO
Fabricante Merz Aesthetics
País de origen Switzerland
Certificación CE marked in accordance with Directive 93/42/EEC relating to medical devices
Composición 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
Volumen / Tamaño 1 ml
Envase 1 x 1 mL
Tamaño de la aguja Two sterile CE-marked single-use 30G ½" needles supplied in the box
Tipo de uso For professional use - qualified practitioners and clinics only
Profundidad de inyección Superficial to mid-dermis for perioral fine lines

Indicaciones y uso profesional

Indicaciones principales

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

Uso profesional

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 tratamiento

  • Perioral fine lines

Perfil del 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.

Cómo 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.

Por qué comprar en Allpara

Allpara ofrece productos BELOTERO originales y verificados de proveedores seleccionados, con trazabilidad completa de lotes y asesoramiento experto. Atendemos a clínicas y profesionales de la estética con productos con certificado CE, entrega rápida en toda la UE desde nuestro almacén en la UE y precios profesionales competitivos. Nuestra prioridad es la seguridad, la satisfacción y los resultados de sus pacientes, con un servicio posventa dedicado para su tranquilidad.

Preguntas frecuentes

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.

/ Especificaciones

La ficha técnica

Categoría
Rellenos dérmicos
Marca
BELOTERO
Laboratorio
Merz Aesthetics
SKU
10091
Formato
1x1mL
Origen
Suiza
Indicación
Lines, folds and volume correction
Uso
Professional use, qualified practitioners
Atributos
/ Detalles del producto

El expediente completo

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.

Merz Aesthetics, país de origen Suiza.

Enviado a toda la UE desde nuestro almacén en la UE, con seguimiento y seguro, y envío en 24-72h. Cada unidad se envía con número de lote y fecha de caducidad, en depósito aduanero de la UE y con trazabilidad de lote.

Conservar según las especificaciones del fabricante, protegido de la luz directa. La cadena de frío solo se utiliza cuando el producto lo requiere.

Condiciones de pago a 30 / 60 / 90 días* disponibles para cuentas verificadas previa aprobación de crédito. Se admite la facturación en EUR, CHF y GBP.

Las condiciones son orientativas y se confirman tras la revisión de la cuenta.

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.

/ Respuestas rápidas

Todo lo que un comprador pregunta primero

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.
/ FAQ

Preguntas frecuentes

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.
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.

Más productos de Merz

Ver laboratorio

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Belotero Soft Lidocaine

En stock
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Inicie sesión o solicite una cuenta B2B para ver su precio.
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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.

Principales ventajas 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
Información clave
Marca BELOTERO
Fabricante Merz Aesthetics
País de origen Switzerland
Certificación CE marked in accordance with Directive 93/42/EEC relating to medical devices
Composición 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
Volumen / Tamaño 1 ml
Envase 1 x 1 mL
Tamaño de la aguja Two sterile CE-marked single-use 30G ½" needles supplied in the box
Tipo de uso For professional use - qualified practitioners and clinics only
Profundidad de inyección Superficial to mid-dermis for perioral fine lines

Indicaciones y uso profesional

Indicaciones principales

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

Uso profesional

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 tratamiento

  • Perioral fine lines

Perfil del 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.

Cómo 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.

Por qué comprar en Allpara

Allpara ofrece productos BELOTERO originales y verificados, con trazabilidad completa de lotes, stock con certificado CE, entrega rápida en toda la UE y servicio posventa experto.

Preguntas frecuentes

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.

Más productos de Merz

Ver el laboratorio →

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.

Merz Aesthetics, país de origen Suiza.

Enviado a toda la UE desde nuestro almacén en la UE, envío en 24-72h, con seguimiento y seguro. Cada unidad se envía con número de lote y fecha de caducidad, en depósito aduanero de la UE y con trazabilidad de lote. Conservar según las especificaciones del fabricante.

Pago a 30 / 60 / 90 días* para cuentas verificadas previa aprobación de crédito. Facturación en EUR, CHF y GBP.

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.

* Producto de uso profesional. El envase puede variar según el lote o el mercado. Consulte las instrucciones de uso suministradas para las indicaciones completas y las contraindicaciones.