Restylane with Lidocaine is a dermal filler that is commonly used for facial rejuvenation, such as to smooth wrinkles and lines, and to restore volume to areas of the face that have lost fullness over time. The addition of lidocaine to Restylane helps to provide a more comfortable treatment experience for patients, as it is a local anesthetic that can help to numb the area being treated.

COMPOSITION

Hyaluronic Acid: 20 mg/ml
Lidocaine: 0.3%

INDICATIONS FOR USE

Restylane with lidocaine is indicated for facial rejuvination of moderate to deep facial line and wrinkles and can also be used in the cheeks, nasal labial folds, tear troughs, undereye and chin.

DURATION

Up to 12 months

FREE SHIPPING within Canada and the continential United States.

DISCLAIMER
Any medical device on this website is intended to be used exclusively by healthcare providers authorized to perform cosmetic injections.

RESTYLANE® Lidocaine

C$260.00

Quantity

Allergy to hyaluronic acid.

For additional information about the product, please refer to the information sheet provided inside the packaging, which contains important details regarding usage instructions, contraindications, and other pertinent information.
Dermal Distributor Outlet is committed to offering only the highest quality Class 3 medical devices (dermal fillers), ensuring that all products sold have undergone rigorous approval processes by Health Canada.

According to Canadian Law, any entity involved in the sale or distribution of Class 3 medical devices (dermal fillers), must possess a valid Medical Device Establishment License (MDEL) issued by Health Canada. The MDEL is a regulatory requirement designed to ensure the safety, quality, and effectiveness of medical devices available in the Canadian market.

The MDEL license demonstrates that the establishment has met the necessary criteria, including but not limited to quality management systems, risk management, adverse event reporting, and compliance with Good Manufacturing Practices (GMP). It signifies that the establishment has undergone the necessary assessments and inspections to comply with the regulatory standards set forth by Health Canada.

It is essential for companies engaged in the sale or distribution of Class 3 medical devices to obtain and maintain a valid MDEL license. Failure to do so may result in penalties, legal implications, and restrictions on the sale and distribution of medical devices within Canada.

Dermal Distributor Outlet, in collaboration with its manufacturing partners, holds valid Medical Device Establishment Licenses (MDELs) issued by Health Canada, demonstrating their commitment to regulatory compliance and ensuring the sale and distribution of authorized Class 3 medical devices.

Validation of MDEL and Health Canada compliance may be obtained accessing the link below:

Health Canada MDEL Listings

RESTYLANE LIDOCAINE

MANUFACTURER: Q-Med AB

Seminariegatan 21, Uppsala, SE 75228

MDEL (Manufacturer): 011501

MDEL (Dermal Distributor Outlet): 23703

RESTYLANE® Lidocaine

Contraindications

Package Contents

Health Canada Approved