Experience Advanced Pre-loaded
IOL Delivery

In cataract surgery, the moment of IOL implantation is crucial. It affects the placement of the IOL, impacts the state of the incision and sets the stage for post-op refractive outcomes.

With the UltraSert Delivery System, you get:

  • Smooth injection*,1,2
  • Preserved incisions1,3
  • Consistent delivery1,3

Explore the data in the tabs below for a closer look at how.

The AcrySof® IQ IOL with the UltraSert™ Pre-loaded IOL Delivery System

Consistent Delivery with the Meticulously Engineered Plunger Tip

In order to promote consistent, precise IOL delivery into the capsular bag, the plunger tip of the UltraSert Pre-loaded System is designed to:

  • Ensure the trailing IOL haptic remains tucked during insertion1,3
  • Extend 6.5 mm past the nozzle without adhering to the IOL1,3
The plunger tip of the UltraSert™ Delivery System

The plunger tip of the UltraSert Delivery System is designed to ensure proper haptic configuration and consistent IOL placement.1,3


Preclinical data support

Unlike other pre-loaded systems tested, the UltraSert System demonstrated both 0% incidence of trapped trailing haptic and IOL adherence to the plunger tip.3

UltraSert™ System demonstrated both 0% incidence of trapped trailing haptic and IOL adherence to the plunger tip.

Non-clinical lab study in porcine eyes comparing the pre-loaded injectable IOL delivery system performance of the UltraSert System, the iTec System and the iSert System and the manual delivery system performance of the MONARCH® III D System (n=10 porcine eyes per group). Study observations included rate of adherence, rate of in-the-bag delivery, IOL/delivery device interactions, optic and haptic unfolding time, rate of cartridge tip splitting and corneal incision size.

*Results of prototype testing of the UltraSert Pre-loaded IOL Delivery System in artificial setting by 42 ophthalmologists and 20 nurses/technicians (US Alcon Market Research, Feb. 2015).
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View Important Product Information for
UltraSert Pre-loaded Delivery System +

ULSTRASERT PRE-LOADED IOL DELIVERY SYSTEM WITH THE ACRYSOF® IQ ASPHERIC IOL IMPORTANT PRODUCT INFORMATION

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.

INDICATIONS: The AcrySof® IQ aspheric intraocular lens (“AcrySof IQ”) is intended for the replacement of the human lens to achieve visual correction of aphakia in adult patients following cataract surgery. This lens is intended for placement in the capsular bag.

WARNING/PRECAUTION: Use the UltraSert Pre-loaded Delivery System (“UltraSert”) at temperatures between 18o C (64o F) and 23oC (73o F). Use only Alcon viscoelastic qualified for this device. Do not use the UltraSert if the nozzle appears damaged or deformed. Follow the Directions for Use for correct order and sequence of steps to avoid damage to the IOL or the UltraSert.

Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting a lens in a patient with any of the conditions described in the Directions for Use. Caution should be used prior to lens encapsulation to avoid lens decentrations or dislocations.

Studies have shown that color vision discrimination is not adversely affected in individuals with the AcrySof® Natural IOL and normal color vision. The effect on vision of the AcrySof® Natural IOL in subjects with hereditary color vision defects and acquired color vision defects secondary to ocular disease (e.g., glaucoma, diabetic retinopathy, chronic uveitis, and other retinal or optic nerve diseases) has not been studied. Do not resterilize; do not store over 45o C.

ATTENTION: Reference the Directions for Use for Model AU00T0 for a complete listing of indications, warnings and precautions.

Click here to view the AcrySof® IQ IOL with the UltraSert Preloaded IOL Delivery System Directions For Use (DFU).

ULSTRASERT PRE-LOADED IOL DELIVERY SYSTEM WITH THE ACRYSOF® IQ ASPHERIC IOL IMPORTANT PRODUCT INFORMATION

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.

INDICATIONS: The AcrySof® IQ aspheric intraocular lens (“AcrySof IQ”) is intended for the replacement of the human lens to achieve visual correction of aphakia in adult patients following cataract surgery. This lens is intended for placement in the capsular bag.

WARNING/PRECAUTION: Use the UltraSert Pre-loaded Delivery System (“UltraSert”) at temperatures between 18o C (64o F) and 23oC (73o F). Use only Alcon viscoelastic qualified for this device. Do not use the UltraSert if the nozzle appears damaged or deformed. Follow the Directions for Use for correct order and sequence of steps to avoid damage to the IOL or the UltraSert.

Careful preoperative evaluation and sound clinical judgment should be used by the surgeon to decide the risk/benefit ratio before implanting a lens in a patient with any of the conditions described in the Directions for Use. Caution should be used prior to lens encapsulation to avoid lens decentrations or dislocations.

Studies have shown that color vision discrimination is not adversely affected in individuals with the AcrySof® Natural IOL and normal color vision. The effect on vision of the AcrySof® Natural IOL in subjects with hereditary color vision defects and acquired color vision defects secondary to ocular disease (e.g., glaucoma, diabetic retinopathy, chronic uveitis, and other retinal or optic nerve diseases) has not been studied. Do not resterilize; do not store over 45o C.

ATTENTION: Reference the Directions for Use for Model AU00T0 for a complete listing of indications, warnings and precautions.

Click here to view the AcrySof® IQ IOL with the UltraSert Preloaded IOL Delivery System Directions For Use (DFU).