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SKU 11134

Saypha Filler Lidocaine

En stock
Volumen
1 x 1 mL
Laboratorio
Croma-Pharma GmbH
Origen
Austria
Indicación
Facial wrinkle correction and lip volume enhancement
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Etiquetas

Saypha Filler Lidocaine is a viscoelastic implant from Croma-Pharma in Austria, developed to correct moderate to severe nasolabial folds and for lip augmentation. It is suitable for practitioners and must be placed in the mid to deep dermis or submucosa. Its cross-linked hyaluronic acid, obtained from Streptococcus equi bacteria, is supplemented with lidocaine hydrochloride and phosphate-buffered at pH 6.7 to 7.3, giving 2.3% sodium hyaluronate (equivalent to 23 mg/mL) with lidocaine HCl 0.3%, for professional use. Each box contains one pre-filled 1.0 mL syringe with two 27G 1/2 inch needles, three patient record labels and an international implant card.

Principales ventajas de Saypha Filler Lidocaine

  • Corrects moderate to severe nasolabial folds and augments the lips
  • Cross-linked sodium hyaluronate at 23 mg/mL, of non-animal origin from Streptococcus equi bacteria
  • Contains lidocaine hydrochloride 0.3%, which reduces pain and discomfort during injection
  • Cross-linked to a mean degree of 0.5 to 1.0% with a typical particle size of approximately 316 micrometres
  • BDDE cross-linking agent present at 2 ppm or less
  • Steam sterilised in the syringe, which serves as the sterile barrier
  • Supplied with two 27G 1/2 inch needles, three patient record labels and an international implant card
  • Manufactured by Croma-Pharma in Austria
Información clave
Marca SAYPHA
Fabricante Croma-Pharma GmbH
País de origen Austria
Certificación CE marked 0123. The needles supplied are CE marked 0197
Composición Cross-linked sodium hyaluronate 2.3%, equivalent to 23 mg/mL, obtained from Streptococcus equi bacteria, with lidocaine hydrochloride 0.3%, sodium chloride 0.75%, disodium phosphate dodecahydrate 0.24%, sodium dihydrogen phosphate dihydrate 0.05% and BDDE cross-linking agent at 2 ppm or less, in water for injection, phosphate buffered at pH 6.7 to 7.3. Mean cross-linking degree 0.5 to 1.0%, typical particle size approximately 316 micrometres
Envase 1 pre-filled syringe x 1.0 mL with two 27G 1/2 inch needles, three patient record labels, an international implant card and a link to the patient information leaflet
Tipo de uso For professional use. Injectable dermal filler with anaesthetic
Volumen / Tamaño 1 x 1 mL
Profundidad de inyección Mid to deep dermis or submucosa
Protocolo / Duración For healthy adults, the maximum total dose of lidocaine hydrochloride should not exceed 300 mg, or 4.5 mg per kg body weight, whichever is less, per session

Indicaciones y uso profesional

Indicaciones principales

  • Moderate to severe nasolabial folds
  • Lip augmentation

Uso profesional

Saypha Filler Lidocaine is intended for an appropriately trained healthcare professional who is qualified or accredited in accordance with national law, and is not intended to be used by lay persons. It is injected into the mid to deep dermis or submucosa. For healthy adults the maximum total dose of lidocaine hydrochloride should not exceed 300 mg, or 4.5 mg per kg body weight, whichever is less, per session; where other forms of lidocaine are used concurrently, whether topical or injected, the maximum total dose must be considered, and the concomitant use of other local anaesthetics or agents structurally related to amide-type anaesthetics should also be taken into account since systemic toxicity may be additive. Patients should avoid strenuous exercise and exposure to extensive sun or heat in the first 48 hours after injection.

Zonas de tratamiento

  • Nasolabial folds, by mid to deep dermis injection
  • Lips, by submucosal injection

Perfil del paciente

For adults 18 years of age or older, assessed as suitable by the treating practitioner. It must not be used in those who tend to develop hypertrophic scars, have pigment disorders or a susceptibility to keloid formation, since treatment may trigger these complications. It must not be used in those known to be hypersensitive to hyaluronic acid, gram-positive bacterial proteins, lidocaine hydrochloride or amide-type local anaesthetics, since treatment may trigger allergic reactions of varying severity. It must not be used in pregnant or breast-feeding women, or in individuals younger than 18 years of age.

Cómo funciona Saypha Filler Lidocaine ​

Saypha Filler Lidocaine works through cross-linked hyaluronic acid at 23 mg/mL, placed in the mid to deep dermis or the lip submucosa, where it adds volume to correct folds and augment the lip. The gel is cross-linked to a mean degree of 0.5 to 1.0% with a typical particle size of approximately 316 micrometres, and the BDDE cross-linking agent is present at 2 ppm or less. The lidocaine hydrochloride at 0.3% is integrated into the implant in an ancillary role to reduce pain and discomfort caused by the injection. It does not change how the gel behaves in tissue.

Por qué comprar en Allpara

Allpara ofrece productos SAYPHA 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

How does Saypha Filler Lidocaine differ from the lidocaine-free Saypha Filler?

The gel concentration is the same at 23 mg/mL. This reference adds lidocaine hydrochloride 0.3% for injection comfort, and is indicated for nasolabial folds and lip augmentation with placement in the mid to deep dermis or submucosa. Where lidocaine is contraindicated, the plain Saypha Filler is the one to order.

How does it differ from Saypha Lips Lidocaine?

Both carry 2.3% sodium hyaluronate with lidocaine 0.3% and share the same registered indication and placement. Saypha Lips Lidocaine additionally documents a cannula option, a 25G x 2 inch or 22G x 2 3/4 inch cannula in place of the needle.

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Saypha Filler Lidocaine

En stock
Precios solo para cuentas verificadas
Inicie sesión o solicite una cuenta B2B para ver su precio.
Solicitar cuenta B2B

Saypha Filler Lidocaine is a viscoelastic implant from Croma-Pharma in Austria, developed to correct moderate to severe nasolabial folds and for lip augmentation. It is suitable for practitioners and must be placed in the mid to deep dermis or submucosa. Its cross-linked hyaluronic acid, obtained from Streptococcus equi bacteria, is supplemented with lidocaine hydrochloride and phosphate-buffered at pH 6.7 to 7.3, giving 2.3% sodium hyaluronate (equivalent to 23 mg/mL) with lidocaine HCl 0.3%, for professional use. Each box contains one pre-filled 1.0 mL syringe with two 27G 1/2 inch needles, three patient record labels and an international implant card.

Principales ventajas de Saypha Filler Lidocaine

  • Corrects moderate to severe nasolabial folds and augments the lips
  • Cross-linked sodium hyaluronate at 23 mg/mL, of non-animal origin from Streptococcus equi bacteria
  • Contains lidocaine hydrochloride 0.3%, which reduces pain and discomfort during injection
  • Cross-linked to a mean degree of 0.5 to 1.0% with a typical particle size of approximately 316 micrometres
  • BDDE cross-linking agent present at 2 ppm or less
  • Steam sterilised in the syringe, which serves as the sterile barrier
  • Supplied with two 27G 1/2 inch needles, three patient record labels and an international implant card
  • Manufactured by Croma-Pharma in Austria
Información clave
Marca SAYPHA
Fabricante Croma-Pharma GmbH
País de origen Austria
Certificación CE marked 0123. The needles supplied are CE marked 0197
Composición Cross-linked sodium hyaluronate 2.3%, equivalent to 23 mg/mL, obtained from Streptococcus equi bacteria, with lidocaine hydrochloride 0.3%, sodium chloride 0.75%, disodium phosphate dodecahydrate 0.24%, sodium dihydrogen phosphate dihydrate 0.05% and BDDE cross-linking agent at 2 ppm or less, in water for injection, phosphate buffered at pH 6.7 to 7.3. Mean cross-linking degree 0.5 to 1.0%, typical particle size approximately 316 micrometres
Envase 1 pre-filled syringe x 1.0 mL with two 27G 1/2 inch needles, three patient record labels, an international implant card and a link to the patient information leaflet
Tipo de uso For professional use. Injectable dermal filler with anaesthetic
Volumen / Tamaño 1 x 1 mL
Profundidad de inyección Mid to deep dermis or submucosa
Protocolo / Duración For healthy adults, the maximum total dose of lidocaine hydrochloride should not exceed 300 mg, or 4.5 mg per kg body weight, whichever is less, per session

Indicaciones y uso profesional

Indicaciones principales

  • Moderate to severe nasolabial folds
  • Lip augmentation

Uso profesional

Saypha Filler Lidocaine is intended for an appropriately trained healthcare professional who is qualified or accredited in accordance with national law, and is not intended to be used by lay persons. It is injected into the mid to deep dermis or submucosa. For healthy adults the maximum total dose of lidocaine hydrochloride should not exceed 300 mg, or 4.5 mg per kg body weight, whichever is less, per session; where other forms of lidocaine are used concurrently, whether topical or injected, the maximum total dose must be considered, and the concomitant use of other local anaesthetics or agents structurally related to amide-type anaesthetics should also be taken into account since systemic toxicity may be additive. Patients should avoid strenuous exercise and exposure to extensive sun or heat in the first 48 hours after injection.

Zonas de tratamiento

  • Nasolabial folds, by mid to deep dermis injection
  • Lips, by submucosal injection

Perfil del paciente

For adults 18 years of age or older, assessed as suitable by the treating practitioner. It must not be used in those who tend to develop hypertrophic scars, have pigment disorders or a susceptibility to keloid formation, since treatment may trigger these complications. It must not be used in those known to be hypersensitive to hyaluronic acid, gram-positive bacterial proteins, lidocaine hydrochloride or amide-type local anaesthetics, since treatment may trigger allergic reactions of varying severity. It must not be used in pregnant or breast-feeding women, or in individuals younger than 18 years of age.

Cómo funciona Saypha Filler Lidocaine ​

Saypha Filler Lidocaine works through cross-linked hyaluronic acid at 23 mg/mL, placed in the mid to deep dermis or the lip submucosa, where it adds volume to correct folds and augment the lip. The gel is cross-linked to a mean degree of 0.5 to 1.0% with a typical particle size of approximately 316 micrometres, and the BDDE cross-linking agent is present at 2 ppm or less. The lidocaine hydrochloride at 0.3% is integrated into the implant in an ancillary role to reduce pain and discomfort caused by the injection. It does not change how the gel behaves in tissue.

Por qué comprar en Allpara

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

Preguntas frecuentes

How does Saypha Filler Lidocaine differ from the lidocaine-free Saypha Filler?

The gel concentration is the same at 23 mg/mL. This reference adds lidocaine hydrochloride 0.3% for injection comfort, and is indicated for nasolabial folds and lip augmentation with placement in the mid to deep dermis or submucosa. Where lidocaine is contraindicated, the plain Saypha Filler is the one to order.

How does it differ from Saypha Lips Lidocaine?

Both carry 2.3% sodium hyaluronate with lidocaine 0.3% and share the same registered indication and placement. Saypha Lips Lidocaine additionally documents a cannula option, a 25G x 2 inch or 22G x 2 3/4 inch cannula in place of the needle.

Más productos de Croma-Pharma

Ver el laboratorio →
* 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.