DUROLANE

Product Description

DUROLANE® is a single-injection hyaluronic acid treatment designed to provide rapid and sustained relief from joint pain associated with osteoarthritis. Manufactured by Bioventus, this injectable gel effectively lubricates and cushions the affected joints, significantly improving patient mobility and comfort. Ideal for use in clinical settings, DUROLANE® is a professional-grade medical solution trusted by healthcare providers for consistent therapeutic outcomes.

DUROLANE® Dosage and Administration

DUROLANE® is supplied as follows:

• A single-use, pre-filled syringe containing 60 mg/3 ml of stabilized hyaluronic acid.

Administration guidelines include:

• Administer via intra-articular injection directly into the affected joint.
• Single injection per treatment session.
• The procedure must be performed by healthcare professionals experienced in joint injections.
• Aseptic technique and standard clinical protocols should be strictly followed during administration.

Ingredient Information

DUROLANE® contains:

• Stabilized hyaluronic acid (60 mg/3 ml), non-animal derived, ensuring biocompatibility and safety.
• Phosphate-buffered saline to maintain product stability and physiological compatibility.

This formulation delivers extended lubrication and effective joint cushioning.

Storage Instructions

• Store between 2°C and 25°C (36°F to 77°F).
• Protect from direct sunlight, moisture, and freezing.
• Keep sealed in the original packaging until ready for use.
• Do not use beyond expiration date or if the packaging integrity is compromised.

Proper storage of orthopedic injections helps maintain the quality, efficacy, and safety of DUROLANE®.

DUROLANE® Contraindications

Avoid using DUROLANE® in patients who:

• Are pregnant or breastfeeding.
• Exhibit known hypersensitivity to hyaluronic acid or other components.
• Have active joint infections or skin lesions at the injection site.
• Are experiencing severe inflammation or autoimmune joint conditions without prior medical consultation.

DUROLANE® Precautions and Warnings

• Administer exclusively in sterile clinical settings by experienced medical professionals.
• Conduct thorough patient evaluations, including allergy assessments, medical history, and current medications.
• Avoid injection into blood vessels and surrounding tissues to prevent complications.
• Clearly instruct patients on post-treatment care, including activities to avoid and signs of potential adverse reactions.

DUROLANE® Manufacturer and Regulatory Information

DUROLANE® is manufactured by Bioventus, a leading international healthcare company specializing in innovative solutions for orthopedics and osteoarthritis management.

• Fully compliant with European (CE-marked) and international regulatory standards.
• Produced under rigorous quality control processes.
• Trusted globally by healthcare providers for safety, consistency, and effectiveness.

Healthcare providers who choose to order DUROLANE® or purchase DUROLANE products from Kinami Health benefit from authentic products, assured clinical efficacy, and comprehensive support to optimize patient outcomes.