BELOTERO referencias disponibles en ALLPARA para uso profesional, de origen directo y certificadas en cada envío.
Belotero Soft Lidocaine
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
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.
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Belotero Soft Lidocaine
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
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.