CE认证
皮肤填充剂
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.
主要优势： 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
适应症与专业用途
主要适应症
- Filling of perioral fine lines
- Injection into the superficial to mid-dermis
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
- Perioral fine lines
适用患者
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.
作用原理： 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.
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 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.
更多产品： Merz
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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.
主要优势： 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
适应症与专业用途
主要适应症
- Filling of perioral fine lines
- Injection into the superficial to mid-dermis
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
- Perioral fine lines
适用患者
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.
作用原理： 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.
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 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.
更多产品： Merz
查看制造商 →* 专业用途产品。包装可能因批次或市场而异。完整的使用说明和禁忌症请参阅随附的使用说明书。