Logo
CelluErase (Cellurase Microsurgical Blades)

CelluErase (Cellurase Microsurgical Blades)

Love Cosmedical

Aesthetic Medical Device
  • Class II medical device for cellulite treatment as indicated by distributors (e.g., ISLA MED).
  • Manufactured in accordance with applicable European medical device regulations and standards for sterile single Use instruments (e.g., ISO 13485 quality management for medical devices, where applicable).
Cellulite treatment microsurgical blade for subcision

Description

CelluErase (also referred to as Cellurase) is a class II medical device from Love Cosmedical consisting of a specially designed microsurgical blade for the treatment of cellulite-related dimpling. The blade is intended to perform controlled subcision of fibrous connective tissue strands that tether the dermis to deeper layers, contributing to the appearance of dimpled, irregular skin. By releasing these fibrous septae, CelluErase helps the skin surface \pop up\ and appear smoother. It is typically used on body areas affected by cellulite, such as thighs and buttocks, and may be combined with mesotherapy products like StrikeCell as part of a comprehensive cellulite treatment protocol. The device is supplied as a sterile, single-use microsurgical blade mounted on a handle and is intended exclusively for use by trained medical or aesthetic professionals.

Bnefits

  • Specifically engineered microsurgical blade for targeting cellulite dimples caused by fibrous connective tissue tethering.
  • Facilitates subcision of fibrous septae to allow the skin surface to rise and appear smoother.
  • Minimally invasive treatment concept compared with more extensive surgical procedures for cellulite.
  • Can be combined with mesotherapy treatments such as StrikeCell by Love Cosmedical to enhance overall cellulite management strategies.
  • Pack of four devices per box provides multiple treatment blades for professional use.
  • Designed as a cost-efficient subcision tool compared with more complex or device-based cellulite treatments.
  • Intended for use by qualified aesthetic and medical practitioners, supporting controlled and targeted treatment in a professional setting.

Indications

  • For professional aesthetic treatment of cellulite-related dimpling lesions on the body.
  • Indicated for use in subcision procedures to release fibrous connective tissue strands that tether the dermis to deeper layers and create a dimpled appearance.
  • Typically used on areas affected by cellulite such as thighs, buttocks and other body regions where localized dimples are present.
  • To be used as part of a professional cellulite reduction protocol, which may include adjunctive mesotherapy with products like StrikeCell.

Composition

  • Microsurgical blade made of surgical steel for precise cutting of fibrous connective tissue.
  • Handle/body manufactured from medical-grade plastic, forming a lightweight, ergonomic instrument.
  • Device dimensions (approximate, based on distributor specification): total length around 14.5 cm, diameter around 0.5 cm, blade length around 2.5 cm.
  • Single-use, sterile packaging for each blade to maintain asepsis until use.

Formulation

  • Non-pharmacological, mechanical class II medical device designed for subcision in cellulite treatment.
  • Non-sterile in terms of active substances (no drug or biologic component); sterility refers to the device packaging and blade.
  • Single-use microsurgical instrument intended for use by trained professionals in an appropriate clinical environment.

Packaging

  • Box containing 4 individually packed CelluErase (Cellurase) microsurgical blades.
  • Each blade supplied in sterile packaging for single use only.
  • Outer carton labelled with product name (CelluErase / Cellurase), manufacturer (Love Cosmedical), quantity (4 devices) and class II medical device status.
  • Intended for distribution to professional users via aesthetic pharmacies and medical distributors.

Usage

  • For use only by doctors or suitably trained aesthetic practitioners experienced in subcision and cellulite treatment.
  • Before use, confirm the integrity of the sterile packaging and check expiry information; do not use if packaging is damaged or compromised.
  • Select appropriate treatment areas presenting cellulite dimples and plan the procedure according to professional training and local guidelines.
  • Using aseptic technique and appropriate local anaesthesia as per clinic protocol, the practitioner introduces the microsurgical blade via a small entry point to reach the fibrous connective tissue septae responsible for skin tethering.
  • Controlled subcision of targeted fibrous bands is performed to release tethering and allow the overlying skin to elevate, aiming to reduce the visible dimpling.
  • The procedure may be combined with mesotherapy treatments such as StrikeCell (Love Cosmedical) according to manufacturer guidance and clinical judgement.
  • After treatment, the device must be disposed of safely as clinical sharps waste; it is strictly single-use and should never be re-sterilised or reused.
  • Follow post-procedure care protocols, including monitoring for bruising, swelling or other local reactions, and advising the patient on aftercare and activity restrictions where appropriate.

Contraindications

  • Use in patients with known bleeding disorders or on anticoagulant/antiplatelet therapy where invasive procedures are contraindicated, unless carefully assessed and cleared by a physician.
  • Presence of active skin infection, inflammation, open wounds or dermatitis at or near the intended treatment site.
  • Known hypersensitivity or allergy to any material used in the device (e.g., components of the plastic handle, surgical steel) where clinically relevant.
  • Patients with uncontrolled systemic diseases or conditions that impair wound healing (e.g., poorly controlled diabetes, severe vascular disorders), unless assessed and approved by the treating physician.
  • Use in pregnant or breastfeeding patients where local regulations, guidelines or practitioner judgement advise against elective aesthetic procedures.
  • Use outside a suitable clinical environment or by untrained, non-medical personnel.

Adverse Effects

  • Expected local reactions such as bruising, swelling, tenderness and mild pain at the treatment site.
  • Transient erythema or skin discolouration in treated areas.
  • Risk of haematoma formation due to disruption of small blood vessels during subcision.
  • Potential for infection if aseptic technique and appropriate aftercare are not strictly followed.
  • Rare risk of contour irregularities, overcorrection or undercorrection if tissue release is excessive or insufficient.
  • Scarring, pigment changes or prolonged induration in the treated area in rare cases.
  • Patient dissatisfaction with cosmetic outcome, as with all aesthetic procedures.

Storage Conditions

  • Store in a cool, dry place away from direct sunlight and excessive heat or humidity.
  • Keep in original packaging until time of use to maintain sterility and protect the blade.
  • Avoid mechanical shock or crushing that could damage the blade or compromise sterile packaging.
  • Keep out of reach of unauthorised personnel and patients; intended only for professional clinical use.
  • Do not use after the expiry date indicated on the packaging.

Duration

The device is used during a single subcision session per treated area; overall treatment course (number of sessions and intervals) is determined by the treating practitioner based on severity of cellulite, treatment plan and patient response.

Onset

A degree of improvement in skin smoothness may be visible once post-procedure swelling and bruising subside; full visual results typically evolve over weeks to months as tissue remodelling occurs, depending on individual factors and adjunctive therapies.

Browse more Aesthetic Medical Device

Top Treatments

Top Cities in the UK