Product Features

1. The intraocular lens material has good biocompatibility and excellent homogeneity. Zero-impurity technology is adopted for the material polymerization. The nanometer numerical control processing technology and proprietary hydration cleaning technology are adopted for production and processing. With high product purity and no glistening, there is no product turbidity and impurity deposition caused by the material after the operation.
2. With modifed C-shaped haptic design, the capsular bag has a large supporting contactangle, which can suit different size capsular bags and provides a guarantee for maintaining the product centering after the operation. It has the sharp angle square edge design, so the product closely adheres to the posterior capsule to form a protective barrier, thereby preventing epithelial cells from migrating to the posterior capsule and reducing the incidence of PCO.

Instruction for Use

1. Examine the type, diopter power, size, the period of validity indicated on the outside package label. DO NOT USE if the expiration date has passed.
2. Take out the tyvek pounch and check that there is no damage on it, verify that lens power, size, type on the vial are same with the data on the outside label.
3. Open the pounch under the aseptic place, open the lens case after final confirmation of lens model and diopter power, take out IOL very carefully and implant IOL into eyes.
4. Rinse the IOL with infusion solution or the equivalent.

Precautions

1. Do not use the One-piece Posterior Chamber Foldable Intraocular Lens if it is after expiration date.
2. Do not try to re-sterilize the One-piece Posterior Chamber Foldable Intraocular Lens.
3. The surgeon must be the person who had observed and assisted IOL implantation surgery many times, must be also the person , who has been ophthalmologist with rich experience and independently completed the IOL omplantation successfully for at least one time.