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Dejale (1x2ml)

Dejale (1x2ml)

Mesorga

Dejale

Dejale is a sterile intradermal gel with 40 mg non-cross-linked hyaluronic acid of medium chain length (1.0–1.5 × 10⁶ Dalton) in a physiological phosphate buffer. Indicated for correcting skin contour irregularities associated with ageing or degenerative changes – biorevitalisation, not volume filling.

  • Non-cross-linked HA
  • 40 mg/2 ml
  • Intradermal

Key benefits

  • Hyaluronic acid in its natural form without cross-linking agent, obtained by fermentation (non-animal).
  • Simple protocol per the IFU: initial course of three treatments one week apart, optionally monthly maintenance.
  • Two sterile 30G ½″ needles and two traceability labels in every box.

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  • Norwegian warehouse
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Description

What it is

Dejale is a sterile, biodegradable, isotonic intradermal gel with non-cross-linked hyaluronic acid of medium chain length (1.0–1.5 × 10⁶ Dalton), obtained from Streptococcus equi and formulated at 40 mg/2 ml in a physiological phosphate buffer. Manufactured by Mesorga S.r.l., Milan.

Mechanism of action

The hyaluronic acid is in its natural form without cross-linking agent and is injected intradermally at medium depth for biorevitalisation and correction of skin contour irregularities. The product is not intended as a volume filler.

Indications and treatment areas

Skin contour irregularities associated with ageing or degenerative changes. Intradermal injection only. Not to be used in combination with laser treatment, chemical peeling or dermabrasion, and no clinical data exist for injection into areas already treated with another filler.

Treatment protocol

  • Technique: linear technique or picotage, intradermally at medium depth, with the supplied 30G ½″ needle.
  • Frequency: initial course of three treatments one week apart, optionally followed by monthly maintenance treatments.
  • Dosage: depends on the wrinkle or depression to be corrected; assessed by the physician.

Expected results

Correction of skin contour irregularities associated with ageing. Inflammatory reactions (redness, oedema) may occur for up to one week after injection.

Documentation and traceability

CE-marked medical device (syringe CE 1984, needles CE 0318). Non-pyrogenic, sterilised by moist heat. The box contains two batch labels for the patient record and the patient. For physician use only. Store at 2–25 °C.

Ingredients and composition

Composition: Sodium hyaluronate 40 mg/2 ml (non-cross-linked, 1.0–1.5 × 10⁶ Dalton, non-animal), sodium chloride, sodium dihydrogen phosphate dihydrate, disodium phosphate dodecahydrate and water for injection. 1 × 2 ml prefilled syringe with 2 × sterile 30G ½″ needles.

Directions and protocol

Initial course of three treatments one week apart, optionally followed by monthly maintenance treatments (manufacturer's IFU).

Specifications

Item no.:50120-B
Classification: CE-marked medical device
Active ingredient: Sodium hyaluronate 40 mg/2 ml, non-cross-linked, non-animal
Molecular weight: 1.0–1.5 × 10⁶ Dalton (medium chain length)
Production: Biological fermentation with Streptococcus equi, sterilised by moist heat
Format: 1 × 2 ml prefilled syringe, 2 × sterile 30G ½″ needles, 2 traceability labels
Intended use: Physiological skin ageing (roughness, reduced radiance, wrinkles) and superficial scars
Protocol: Initial course: 3 treatments one week apart, optionally monthly maintenance (manufacturer's IFU)
Manufacturer: Mesorga S.r.l., Milan, Italy

Documentation and compliance

CE-marked medical device

LOT number and Declaration of Conformity accompany every shipment for your patient records.

The product information below is reserved for approved clinics. Log in

Shipping and returns

Ships from our Norwegian warehouse, typically 1 to 2 business days.

Sterile and lot-controlled goods cannot be returned for patient-safety reasons. Contact us for defects or transit damage.

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Frequently asked questions

What is the difference between Dejale and an HA filler?

Dejale contains non-cross-linked hyaluronic acid in its natural form and is injected intradermally for biorevitalisation and correction of skin contour irregularities. A cross-linked filler is formulated to add volume. Dejale is not a volume product.

Which injection techniques does the IFU describe?

The IFU specifies linear technique or picotage, intradermally at medium depth, with the supplied 30G ½″ needle. The product must only be used by physicians with specific training in the injection technique, and must not be injected into blood vessels, bone, tendons, ligaments, muscles or moles.

Can Dejale be combined with other aesthetic treatments?

No – not in the same treatment. The IFU states that Dejale must not be used in combination with laser treatment, chemical peeling or dermabrasion. There are also no clinical data for injection into an area already treated with another filler.

What are the contraindications for Dejale?

Not to be used in patients prone to hypertrophic scarring, with autoimmune disease or on immunotherapy, with known hypersensitivity to hyaluronic acid, in pregnant or breastfeeding women, or in patients under 18. Patients on anticoagulants or antiplatelet agents should consult a physician. Not to be used in areas with inflammatory or infectious skin processes (e.g. acne, herpes). Possible side effects: redness, oedema and tenderness for up to one week, nodules if placed too superficially, discolouration.

Compare products

This productDejale (1x2ml) Ejal40 (1x2ml) Profhilo
Price
Manufacturer MesorgaEjal40IBSA
Availability In stockIn stockIn stock
CE marking CE markedCE markedCE marked
Classification CE-marked medical device CE-marked medical device (CE 1984)CE-marked medical device (CE 0373)
Active ingredient Sodium hyaluronate 40 mg/2 ml, non-cross-linked, non-animal –Sodium hyaluronate (H-HA + L-HA), without chemical modification
Format 1 × 2 ml prefilled syringe, 2 × sterile 30G ½″ needles, 2 traceability labels –1 × 2 ml pre-filled syringe
Intended use Physiological skin ageing (roughness, reduced radiance, wrinkles) and superficial scars Physiological skin ageing (roughness, reduced radiance, wrinkles) and superficial scars–
Manufacturer Mesorga S.r.l., Milan, Italy Medixa Srl, Via Figliola 57, 80040 S. Sebastiano al Vesuvio (NA), ItalyIBSA Farmaceutici Italia srl, Italy
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