PERFECTHA® DERM

Where can I buy this product?

PERFECTHA® DERM may be available for purchase through Health Supplies Plus by licensed medical practitioners holding a valid medical license, for use only where legally permissible according to local and national regulations. First-time buyers can register an online account by providing required professional information, including medical license verification and a valid shipping address. Account verification is typically completed within 2 business hours, after which you can purchase medical supplies at competitive wholesale pricing. Registered members may also be eligible for volume discounts and receive dedicated customer service support. It is the practitioner’s sole responsibility to ensure compliance with all regulatory requirements regarding the purchase and use of medical devices in their jurisdiction.

Product Information

What is PERFECTHA® DERM?

PERFECTHA® DERM is a sterile, viscoelastic, injectable gel composed of cross-linked hyaluronic acid (HA) of non-animal origin, manufactured by Sinclair Pharma (France). It utilizes Sinclair’s proprietary E-brid™ technology, stated by the manufacturer to create a structured HA gel with claimed low levels of residual BDDE cross-linking agent.

This formulation is designed as a versatile mid-range filler, typically containing 20mg/mL of hyaluronic acid. It is intended for injection into the mid-dermis to correct moderate wrinkles and folds, as well as for lip augmentation. This formulation does not contain lidocaine.

Storage: Store according to manufacturer guidelines, typically between 2°C and 30°C (36°F and 86°F). Do not freeze. Protect from light.

Authenticity: Health Supplies Plus guarantees that PERFECTHA® products sourced are authentic from the manufacturer or authorized distributors.

Note: For professional use only by trained and licensed practitioners in jurisdictions where its use is legally permitted.

How does PERFECTHA® DERM work?

PERFECTHA® DERM is engineered using E-brid™ technology to function as a filler suitable for moderate corrections. When injected into the mid-dermis, the cross-linked HA gel physically adds volume to lift and smooth moderate wrinkles and folds, such as nasolabial folds or marionette lines.

Its properties are also intended to be suitable for augmenting the lips, providing volume and definition. The manufacturer claims the E-brid™ process contributes to the gel’s integration and performance. The hydrophilic nature of HA helps maintain local skin hydration.

Treatment results are intended to be visible immediately. The manufacturer suggests a duration of effect lasting approximately 6 to 12 months, though individual results will vary based on patient factors, injection site, volume, and technique. As this product is lidocaine-free, appropriate anesthesia (e.g., topical, dental block for lips) should be considered for patient comfort.

Indications for Use

Based on manufacturer information and common use outside the US, PERFECTHA® DERM is typically indicated for adults seeking correction of moderate facial lines and lip enhancement:

• Correction of moderate wrinkles and folds (e.g., nasolabial folds, marionette lines).
• Treatment of glabellar lines (requires specific expertise).
• Lip augmentation for volume and definition.

Appropriate patient selection and correct injection depth (mid-dermis) are crucial where its use is permitted.

Primary Benefits

• Versatile filler designed for moderate wrinkles, folds, and lip augmentation.
• Utilizes E-brid™ technology (claimed low residual BDDE).
• Provides immediate volumizing and smoothing results.
• Results claimed to last 6-12 months.
• Lidocaine-free formulation.

Side Effects and Safety Information

Common side effects expected with HA filler injections include temporary, injection-site related reactions:

• Swelling
• Bruising
• Redness
• Tenderness or Pain
• Itching
• Firmness or Lumps/Bumps
• Increased Sensitivity

Severe Adverse Events:
As with any dermal filler injection, there are risks of more serious complications. Practitioners must be prepared to manage adverse events. Potential severe adverse events include:

• Vascular Occlusion (VO): Accidental injection into a blood vessel can obstruct blood flow, potentially leading to tissue necrosis (tissue death), scarring, or (in rare cases involving facial arteries, especially labial or glabellar) blindness or stroke. Prompt recognition and management protocols are crucial.
• Severe allergic reactions or hypersensitivity to HA
• Inflammation, infection, or abscess formation
• Granuloma or persistent nodule formation
• Migration of filler
• Prolonged pain or numbness
• Herpetic eruptions (cold sores) in susceptible individuals
• Hematomas

Any signs of vascular compromise, infection, hypersensitivity, or persistent adverse reactions require immediate medical evaluation.