Description
Clinical Description
PRO INFUSION DERM – LUER LOCK – ACQUA is a sterile, single-use micro-infusion delivery device developed for professional aesthetic medicine procedures. The device is designed to facilitate controlled superficial micro-implantation of aesthetic formulations through a multi-needle delivery platform connected via a secure Luer Lock attachment system.
The ACQUA version belongs to the Promoitalia Pro Infusion Derm range and incorporates multiple ultra-fine micro-needles intended to support uniform distribution of compatible injectable or topical aesthetic formulations across the treatment area. The Luer Lock connection enhances stability between the device and compatible syringes, helping practitioners maintain controlled product delivery during treatment.
As a delivery device rather than an injectable product itself, PRO INFUSION DERM – LUER LOCK – ACQUA contains no pharmacologically active ingredients. Treatment outcomes depend on the formulation used in conjunction with the device and the clinical judgement of the practitioner.
What PRO INFUSION DERM – LUER LOCK – ACQUA Is Similar To
PRO INFUSION DERM – LUER LOCK – ACQUA belongs to the category of sterile micro-infusion and microneedling-assisted delivery systems. It may be compared with other professional multi-needle infusion devices used for superficial aesthetic applications.
For clinical orientation, practitioners may compare it with systems such as automated mesotherapy injectors or other sterile micro-infusion platforms designed to improve distribution of aesthetic formulations. Unlike injectable skin boosters such as Profhilo® or Sunekos®, which are injectable products containing active ingredients, PRO INFUSION DERM – LUER LOCK – ACQUA functions solely as a delivery device and does not contain hyaluronic acid, amino acids, or regenerative compounds itself.
Its principal role is to facilitate controlled product placement through multiple micro-needles, whereas skin boosters derive their effect from their active ingredients. Treatment outcomes therefore depend largely on the compatible formulation selected by the practitioner.
This comparison is provided for clinical orientation only and does not imply interchangeability.
Treatment Areas / Indications
Publicly available manufacturer information indicates use for superficial aesthetic delivery procedures and micro-implantation treatments.
Potential treatment areas may include:
- Face
- Neck
- Décolletage
Specific treatment indications ultimately depend on the injectable or aesthetic formulation used alongside the device.
Where additional treatment areas are required, practitioners should refer to the accompanying product documentation and the IFU of the formulation being administered.
Usage / Administration (IFU-Only Section)
Connection type: Luer Lock compatible.
Needle gauge: 30G micro-needles.
Number of micro-needles: 20 micro-needles.
Professional-use statement: Intended for use by qualified medical professionals under appropriate aseptic conditions.
Reuse: Single-use sterile device; do not reuse.
Some practitioners apply specific micro-implantation techniques with this device; these methods are not included in the manufacturer’s official IFU guidance and should not replace official instructions.
Ingredient List
PRO INFUSION DERM – LUER LOCK – ACQUA is a medical device and does not contain injectable active ingredients.
Materials publicly disclosed include:
- Medical-grade stainless steel micro-needles
- Medical-grade polymer components
- Luer Lock connection system
Presentation & Longevity
Presentation
- 1 × sterile single-use PRO INFUSION DERM – LUER LOCK – ACQUA device
- Individually packaged in sterile blister packaging
Longevity
Not applicable. The product is a disposable delivery device rather than a long-lasting implantable or injectable treatment.
Safety Notes / Contraindications
- Single-use only; do not reuse or re-sterilise.
- Do not use if sterile packaging is damaged or opened before use.
- Dispose of according to local regulations governing medical sharps and clinical waste.
- Use only with compatible Luer Lock systems and intended professional aesthetic products.
Where specific contraindications are not disclosed by the manufacturer, practitioners should additionally observe standard clinical precautions.
Regulatory Status
Publicly available documentation identifies the product as a sterile professional-use medical device.
FAQ
1. What is PRO INFUSION DERM – LUER LOCK – ACQUA?
PRO INFUSION DERM – LUER LOCK – ACQUA is a sterile, single-use micro-infusion device designed for professional aesthetic procedures. It features multiple 30G micro-needles and a secure Luer Lock attachment system intended to support controlled and uniform delivery of compatible formulations during superficial aesthetic treatments.
2. Does the device contain hyaluronic acid or active ingredients?
No. PRO INFUSION DERM – LUER LOCK – ACQUA is a delivery device rather than an injectable formulation. It does not contain hyaluronic acid, peptides, amino acids, or regenerative compounds. Clinical outcomes depend on the formulation used alongside the device.
3. How is the device administered?
According to publicly available manufacturer information, the device is connected through a Luer Lock system and used by qualified professionals during superficial micro-infusion procedures. Injection depth, volume per point, and treatment frequency are not provided by the manufacturer in publicly available documentation.
4. Is PRO INFUSION DERM – LUER LOCK – ACQUA reusable?
No. The device is supplied sterile for single-patient use and should be disposed of after treatment according to local sharps disposal regulations. Reuse or re-sterilisation is not recommended because it may compromise device integrity and sterility.
5. How does it compare with skin boosters?
Skin boosters such as Profhilo® and Sunekos® are injectable formulations containing active ingredients designed to affect skin hydration or tissue quality. PRO INFUSION DERM – LUER LOCK – ACQUA functions as a delivery platform only and does not exert a biological effect independently. Any clinical outcome depends on the formulation selected by the practitioner.
