Belotero Volume Lidocaine by Merz Aesthetics is the volumising grade of the BELOTERO range, a hyaluronic acid dermal filler supplied with lidocaine in the syringe and developed for severe nasolabial folds and to enhance the cheeks, the temples and the chin. Injection is into the deep subcutaneous layers or on top of the periosteum, with effects lasting up to 18 months in the nasolabial folds and up to 12 months in the cheeks, temples and chin. Each 1 mL contains sodium hyaluronate 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), and lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7, which makes it the most concentrated grade in the range. Belotero Volume filler is supplied as 2 x 1 mL, a two-syringe pack rather than the single syringe used across most of the range.
主要优势: Belotero Volume Lidocaine
- The volumising grade of the range, placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, temples and chin and to treat severe nasolabial folds
- Sodium hyaluronate 26 mg/ml with lidocaine hydrochloride 3.0 mg/ml, the most concentrated grade in the range
- Cross-linked using 1,4-butanediol diglycidyl ether (BDDE) in a physiological phosphate buffer at pH 7
- Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin
- Contains lidocaine to reduce the sensation of pain and improve comfort during injection
- Supplied as a 2 x 1 mL pack, a two-syringe unit rather than the single syringe used across most of the range
- CE marked 0123
适应症与专业用途
主要适应症
- Enhancement of the cheeks
- Enhancement of the temples
- Enhancement of the chin
- Treatment of severe nasolabial folds
专业用途
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.
治疗部位
- Cheeks
- Temples
- Chin
- Nasolabial folds
适用患者
Suitable for adult patients assessed as appropriate by the treating practitioner. The product is contraindicated 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.
作用原理: Belotero Volume Lidocaine
Belotero Volume Lidocaine works through sodium hyaluronate at 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), with lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7. As the volumising grade it acts as an injectable biodegradable implant placed in the deep subcutaneous layers or above the periosteum, which is why it is directed at the cheeks, temples and chin and at severe nasolabial folds rather than at fine lines. The lidocaine is included to reduce the sensation of pain and improve comfort during injection, and does not alter that mechanism.
为什么选择在 Allpara 订购
Allpara 提供正品、经过验证的 BELOTERO 产品,来自经过严格审核的供应商,具备完整的批次可追溯性和专家支持。我们为诊所和医美专业人士提供CE认证产品、从欧盟仓库快速配送至欧盟各地,以及具有竞争力的专业价格。我们关注的是您患者的安全、满意度和效果,并提供专属售后支持,让您安心无忧。
常见问题
Which BELOTERO grade is Belotero Volume Lidocaine?
Belotero Volume Lidocaine is the volumising grade, supplied at 26 mg/ml sodium hyaluronate with lidocaine hydrochloride 3.0 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE). At 26 mg/ml it is the most concentrated grade in the range and is placed in the deep subcutaneous layers or above the periosteum. Grades are not interchangeable.
Which treatment areas is Belotero Volume Lidocaine used for?
It is placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, the temples and the chin, or to treat severe nasolabial folds. Area selection and placement depth are the treating practitioner's decisions.
How long do the effects of Belotero Volume Lidocaine last?
Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Duration varies with the patient, the area treated, the volume placed and the injection technique.
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Belotero Volume Lidocaine by Merz Aesthetics is the volumising grade of the BELOTERO range, a hyaluronic acid dermal filler supplied with lidocaine in the syringe and developed for severe nasolabial folds and to enhance the cheeks, the temples and the chin. Injection is into the deep subcutaneous layers or on top of the periosteum, with effects lasting up to 18 months in the nasolabial folds and up to 12 months in the cheeks, temples and chin. Each 1 mL contains sodium hyaluronate 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), and lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7, which makes it the most concentrated grade in the range. Belotero Volume filler is supplied as 2 x 1 mL, a two-syringe pack rather than the single syringe used across most of the range.
主要优势: Belotero Volume Lidocaine
- The volumising grade of the range, placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, temples and chin and to treat severe nasolabial folds
- Sodium hyaluronate 26 mg/ml with lidocaine hydrochloride 3.0 mg/ml, the most concentrated grade in the range
- Cross-linked using 1,4-butanediol diglycidyl ether (BDDE) in a physiological phosphate buffer at pH 7
- Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin
- Contains lidocaine to reduce the sensation of pain and improve comfort during injection
- Supplied as a 2 x 1 mL pack, a two-syringe unit rather than the single syringe used across most of the range
- CE marked 0123
适应症与专业用途
主要适应症
- Enhancement of the cheeks
- Enhancement of the temples
- Enhancement of the chin
- Treatment of severe nasolabial folds
专业用途
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.
治疗部位
- Cheeks
- Temples
- Chin
- Nasolabial folds
适用患者
Suitable for adult patients assessed as appropriate by the treating practitioner. The product is contraindicated 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.
作用原理: Belotero Volume Lidocaine
Belotero Volume Lidocaine works through sodium hyaluronate at 26 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE), with lidocaine hydrochloride 3.0 mg/ml in a physiological phosphate buffer at pH 7. As the volumising grade it acts as an injectable biodegradable implant placed in the deep subcutaneous layers or above the periosteum, which is why it is directed at the cheeks, temples and chin and at severe nasolabial folds rather than at fine lines. The lidocaine is included to reduce the sensation of pain and improve comfort during injection, and does not alter that mechanism.
为什么选择在 Allpara 订购
Allpara 提供正品、经过验证的 BELOTERO 产品,具备完整的批次可追溯性、CE认证库存、欧盟范围内快速配送以及专业的售后支持。
常见问题
Which BELOTERO grade is Belotero Volume Lidocaine?
Belotero Volume Lidocaine is the volumising grade, supplied at 26 mg/ml sodium hyaluronate with lidocaine hydrochloride 3.0 mg/ml, cross-linked using 1,4-butanediol diglycidyl ether (BDDE). At 26 mg/ml it is the most concentrated grade in the range and is placed in the deep subcutaneous layers or above the periosteum. Grades are not interchangeable.
Which treatment areas is Belotero Volume Lidocaine used for?
It is placed in the deep subcutaneous layers or above the periosteum to enhance the cheeks, the temples and the chin, or to treat severe nasolabial folds. Area selection and placement depth are the treating practitioner's decisions.
How long do the effects of Belotero Volume Lidocaine last?
Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Duration varies with the patient, the area treated, the volume placed and the injection technique.