RRS XL Hair

RRS

Injectable Aesthetic Treatment

Mesotherapy / Scalp & Hair Biorevitalising Solution

Class III CE Marked medical device for injectable mesotherapy use.
Manufactured in conformity with applicable EU medical device regulations.
Biotechnological, non Animal origin hyaluronic acid.
Produced under medical device quality management systems (e.g. ISO Compliant manufacturing).

Class III CE Marked medical device for injectable mesotherapy use.
Manufactured in conformity with applicable EU medical device regulations.
Biotechnological, non Animal origin hyaluronic acid.
Produced under medical device quality management systems (e.g. ISO Compliant manufacturing).

Mesotherapy / Scalp & Hair Biorevitalising Solution

Description

RRS XL Hair is a CE Class III injectable mesotherapy solution specifically developed to biostimulate hair growth and revitalise the scalp. Based on non-cross-linked hyaluronic acid in a multi-ingredient biorevitalising buffer (amino acids, trace elements, vitamins, terpenes, fatty acids, peptide growth factors and antioxidants), it restructures the scalp extracellular matrix, improves microcirculation and enhances nourishment of hair follicles. This leads to thicker, denser and healthier hair, while helping to prevent and treat hair loss and baldness. RRS XL Hair can be injected in the scalp, eyebrows and pubic area and is designed exclusively for professional use by trained medical practitioners.

Bnefits

Biostimulates hair growth and helps treat hair loss, thinning hair and bald patches.
Strengthens hair follicles and roots, helping to reduce excessive hair shedding.
Improves overall hair density, thickness, shine and structure.
Deeply hydrates and revitalises the scalp thanks to non-cross-linked hyaluronic acid.
Supports restructuring of the intercellular matrix, enhancing nutrient supply to hair roots.
Multi-ingredient cocktail (amino acids, vitamins, trace elements, terpenes, fatty acids, antioxidants, growth factors) nourishes the scalp and follicles.
Can be used on scalp, eyebrows and pubic area for localised hair concerns.
Suitable as both a corrective and preventative treatment against hair loss.
Provides long-lasting improvement in hair quality when used in a structured treatment course.
CE Class III medical device manufactured in accordance with EU medical device regulations.

Indications

Diffuse or patterned hair loss (androgenetic and other alopecia patterns) as part of a mesotherapy protocol.
Thinning, dull or light hair lacking density and vitality.
Hair in poor condition (brittle, weakened, structurally damaged).
Excessive hair shedding and symptomatic hair loss.
Scalp revitalisation and improvement of scalp hydration and health.
Eyebrow atrophy or sparse eyebrows.
Localised hairless areas where stimulation of hair growth is desired (including pubic region).
Preventative treatment in patients at risk of hair thinning or early hair loss.

Composition

Non-cross-linked hyaluronic acid 3 mg/ml (0.3%) of non-animal, biotechnological origin.
17 amino acids (building blocks for keratin and dermal proteins).
9 trace elements (including silicon, iron, magnesium and others).
7 vitamins (including antioxidant and hair-supportive vitamins).
5 terpenes.
1 GM peptide.
3 antioxidants.
2 flavonoids.
2 fatty acids.
1 sodium DNA (nucleotides).
1 FGF (fibroblast growth factor).

Formulation

Sterile, pyrogen-free Class III CE-marked dermal implant / mesotherapy solution.
Non-cross-linked hyaluronic acid 3 mg/ml in an aqueous biorevitalising buffer.
Multi-ingredient cocktail: amino acids, trace elements, vitamins, terpenes, fatty acids, peptide and growth factors, antioxidants and flavonoids.
Lidocaine-free formulation.
Intended for intradermal or very superficial (subepidermal) injection into the scalp and other hair-bearing areas.

Packaging

Standard box: 6 ampoules x 5 ml each (total 30 ml).
Glass ampoules, single-use and sterile.
Outer carton with batch number, expiry date and CE Class III medical device marking.
Professional Instructions for Use (IFU) supplied with the pack.

Usage

For professional use only; must be administered by a qualified physician or suitably trained medical professional in an appropriate clinical setting.
Before treatment, assess patient medical history, hair-loss pattern and scalp condition; obtain informed consent.
Inspect packaging and ampoules; do not use if packaging is damaged, ampoule is cracked or solution is discoloured or contains particles.
Cleanse and disinfect the scalp or treatment area thoroughly in accordance with aseptic technique.
Use a fine mesotherapy needle (typically 30G–32G) for intradermal or very superficial subepidermal injections.
Inject small micro-deposits across the treatment area (scalp, eyebrows or pubic region) using nappage or point-by-point technique, spacing injections approximately 0.5–1 cm apart.
Recommended protocol: apply once or twice per week for a period of 4 to 12 weeks, depending on severity of hair loss and clinical response.
Total volume per session is adjusted according to the area treated; one 5 ml ampoule is generally sufficient for a full scalp session.
For prevention or maintenance, repeat treatment cycles can be performed as needed after the initial course, according to practitioner judgement and patient response.
Advise patients to avoid washing the scalp, using aggressive hair products, or exposing the treated area to intense heat (sauna, steam bath, sunbeds) for at least 24 hours after each session.
Instruct patients to report any persistent pain, swelling, redness, nodules or signs of infection promptly.
Discard any unused solution after opening an ampoule; do not reuse. Dispose of all needles, syringes and ampoules in approved sharps containers.

Contraindications

Known hypersensitivity or allergy to hyaluronic acid, any of the listed components (e.g. amino acids, vitamins, trace elements, peptides, growth factors) or excipients.
Active infections, inflammation, dermatitis or scalp diseases in the proposed treatment area (e.g. folliculitis, psoriasis flare, severe seborrhoeic dermatitis) until resolved.
Autoimmune diseases or patients receiving immunosuppressive therapy, unless the risk–benefit has been carefully evaluated by the practitioner.
Uncontrolled systemic diseases (e.g. uncontrolled diabetes, severe cardiovascular disorders) that may impair healing or increase risk of complications.
Known tendency to keloid or hypertrophic scar formation in the treatment region.
History of severe allergic reactions or anaphylaxis to injectable products.
Pregnancy and breastfeeding (elective aesthetic mesotherapy is generally not recommended in these populations).
Use in children or adolescents under 18 years of age.
Do not inject into blood vessels, areas with permanent fillers, or into infected or necrotic tissue.

Adverse Effects

Common transient injection-site reactions: redness, swelling, tenderness, itching, mild pain or pinpoint bleeding.
Bruising or haematoma formation, particularly in patients taking anticoagulant or antiplatelet medication.
Temporary papules, small nodules or induration at injection sites, usually resolving spontaneously or after gentle massage.
Rare risk of local infection or abscess if aseptic technique is not strictly followed.
Possible allergic or hypersensitivity reactions to one or more components, manifesting as prolonged erythema, oedema, pruritus or induration.
Very rare but serious complications if inadvertently injected intravascularly, potentially leading to vascular compromise and tissue necrosis; these require immediate emergency management.
Post-inflammatory hyperpigmentation may occur in predisposed individuals if there is significant inflammation or inadequate sun protection after treatment.

Storage Conditions

Store in a cool, dry place at controlled room temperature (typically between 2°C and 25–30°C, as indicated on the packaging).
Protect from direct sunlight and excessive heat.
Do not freeze.
Keep ampoules in their original carton until use to maintain sterility and protect from light.
Do not use after the expiry date printed on the ampoule and outer packaging.
Keep out of the reach and sight of children.

Duration

Typical course consists of once or twice weekly sessions for 4 to 12 weeks. Additional or maintenance courses may be repeated as required based on the patient\u2019s hair condition and the practitioner\u2019s clinical assessment.

Onset

Initial improvements in scalp hydration and hair quality may be noticeable within the first few weeks; visible increases in hair density, strength and reduction in shedding are generally expected over 4 to 12 weeks of regular treatment.