PURELON 1.8 %

Cohesive Ophthalmic Viscosurgical Device (OVD)

Overview

PURELON 1.8% represents the next level of cohesive viscoelastic performance.

With 18 mg/mL sodium hyaluronate of 3,200,000 Daltons molecular weight, it provides superior protection of corneal endothelium, outstanding space maintenance, and unmatched clarity during all stages of cataract and anterior segment surgery.

Designed for longer and complex procedures, it ensures smooth manipulation and reliable intraocular pressure control.

Technical Specifications

Composition: Sodium Hyaluronate in Phosphate Saline Buffer Colorless, clear, sterile, non-pyrogenic.

HA Concentration: 18 mg/mL (1.8 %)

Molecular Weight: 3,200,000 Daltons

Classification: Cohesive

Viscosity: 400,000-600,000 mPa·s

pH: 6.8 – 7.6

Osmolality: 280 – 400 mOsm/kg

Storage Temperature: +2 °C to +25 °C

Shelf Life: 36 months

Packaging: 0.55 / 0.85 / 1.0 / 1.5 mL prefilled glass syringe in sterile blister – includes patient labels & IFU

Usage Condition: Ready to use — no pre-cooling required

Key Features

  • High-viscosity cohesive OVD for demanding surgical procedures

  • Provides maximum chamber depth and shape stability

  • Exceptional optical clarity and corneal protection

  • Long-lasting viscoelastic retention

  • Sterile, single-use glass syringe with smooth injectability

Recommended Use

PURELON 1.8% is recommended for advanced and prolonged surgeries, including phacoemulsification and IOL implantation, where maximum stability and tissue protection are required.

Interested in PURELON 1.8 % for your practice?

Contact us to request product details, technical documents, or distributor information.