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SKU 10092

Belotero Volume Lidocaine

Dostępny
Objętość
2 x 1 mL
Laboratorium
Merz Aesthetics
Pochodzenie
Szwajcaria
Wskazanie
Lines, folds and volume correction
Cena hurtowa i historia tylko dla zweryfikowanych
allpara zaopatruje licencjonowanych specjalistów. Zaloguj się lub załóż konto B2B, aby zobaczyć aktualne ceny, progi ilościowe i historię cen.

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.

Najważniejsze zalety: 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
Najważniejsze informacje
Marka BELOTERO
Producent Merz Aesthetics
Kraj pochodzenia Switzerland
Certyfikacja CE marked 0123
Skład Sodium hyaluronate 26 mg/ml and lidocaine hydrochloride 3.0 mg/ml, in physiological phosphate buffer pH 7. The sodium hyaluronate is cross-linked using 1,4-butanediol diglycidyl ether (BDDE)
Objętość / Rozmiar 1 ml
Opakowanie 2 x 1 mL
Rozmiar igły Each syringe is supplied with two sterile CE-marked single-use needles, 27G ½" and 30G ½"
Rodzaj zastosowania For professional use - qualified practitioners and clinics only
Głębokość iniekcji Deep subcutaneous layers or above the periosteum (supraperiosteal), for enhancement of the cheeks, temples and chin and for severe nasolabial folds
Protokół / Czas trwania Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Maximum 8 mL per session, with a recommended maximum of 8 mL in the cheeks, 6 mL in the temples, 4 mL in the nasolabial folds and 5 mL in the chin. Treatment may be renewed within a year without exceeding an annual dose of 16 mL, and sessions in the same area must be spaced at least 2 weeks apart

Wskazania i zastosowanie profesjonalne

Główne wskazania

  • Enhancement of the cheeks
  • Enhancement of the temples
  • Enhancement of the chin
  • Treatment of severe nasolabial folds

Zastosowanie profesjonalne

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.

Obszary zabiegowe

  • Cheeks
  • Temples
  • Chin
  • Nasolabial folds

Profil pacjenta

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.

Jak działa 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.

Dlaczego warto zamawiać w Allpara

Allpara oferuje oryginalne, sprawdzone produkty BELOTERO od zweryfikowanych dostawców, z pełną identyfikowalnością partii i wsparciem ekspertów. Obsługujemy kliniki i specjalistów medycyny estetycznej, oferując produkty z certyfikatem CE, szybką dostawę na terenie całej UE z naszego magazynu w UE oraz konkurencyjne ceny hurtowe. Najważniejsze są dla nas bezpieczeństwo, satysfakcja i efekty Twoich pacjentów - z dedykowanym wsparciem posprzedażowym dla Twojego spokoju.

Najczęściej zadawane pytania

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.

Więcej od Merz

Zobacz laboratorium

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Belotero Volume Lidocaine

Dostępny
Oznaczenie CE Oznaczenie CE Belotero Volume Lidocaine
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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.

Najważniejsze zalety: 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
Najważniejsze informacje
Marka BELOTERO
Producent Merz Aesthetics
Kraj pochodzenia Switzerland
Certyfikacja CE marked 0123
Skład Sodium hyaluronate 26 mg/ml and lidocaine hydrochloride 3.0 mg/ml, in physiological phosphate buffer pH 7. The sodium hyaluronate is cross-linked using 1,4-butanediol diglycidyl ether (BDDE)
Objętość / Rozmiar 1 ml
Opakowanie 2 x 1 mL
Rozmiar igły Each syringe is supplied with two sterile CE-marked single-use needles, 27G ½" and 30G ½"
Rodzaj zastosowania For professional use - qualified practitioners and clinics only
Głębokość iniekcji Deep subcutaneous layers or above the periosteum (supraperiosteal), for enhancement of the cheeks, temples and chin and for severe nasolabial folds
Protokół / Czas trwania Effects last up to 18 months for nasolabial folds and up to 12 months for the cheeks, temples and chin. Maximum 8 mL per session, with a recommended maximum of 8 mL in the cheeks, 6 mL in the temples, 4 mL in the nasolabial folds and 5 mL in the chin. Treatment may be renewed within a year without exceeding an annual dose of 16 mL, and sessions in the same area must be spaced at least 2 weeks apart

Wskazania i zastosowanie profesjonalne

Główne wskazania

  • Enhancement of the cheeks
  • Enhancement of the temples
  • Enhancement of the chin
  • Treatment of severe nasolabial folds

Zastosowanie profesjonalne

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.

Obszary zabiegowe

  • Cheeks
  • Temples
  • Chin
  • Nasolabial folds

Profil pacjenta

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.

Jak działa 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.

Dlaczego warto zamawiać w Allpara

Allpara oferuje oryginalne, sprawdzone produkty BELOTERO z pełną identyfikowalnością partii, produktami z certyfikatem CE, szybką dostawą na terenie całej UE i fachowym wsparciem posprzedażowym.

Najczęściej zadawane pytania

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.

Więcej od Merz

Zobacz laboratorium →
* Produkt do użytku profesjonalnego. Opakowanie może się różnić w zależności od partii lub rynku. Pełne zalecenia i przeciwwskazania znajdziesz w dołączonej instrukcji użycia (IFU).