UltraSert Pre-loaded IOL Delivery System Technology Overview1-3

Device Features

The unique features of the UltraSert™ Delivery System are designed to deliver multiple benefits for the implantation process.

Specifications


AcrySof® IQ IOL with the UltraSert Pre-loaded Delivery System
Model Number
AU00T0
Material
Basell PD702 Polypropylene
System type
Single-use
Delivery technology
TensionGlide plunger
Compatible incision sizes
2.2–3.2 mm
Recommended time to advance for inspection
≥ 7 seconds
Recommended time between advancement and implantation
≤ 3 minutes
Recommended time to advance for implantation
≥ 5 seconds
AcrySof® IQ IOL
Optic type
Aspheric
Optic diameter
6.0 mm
Overall length
13.0 mm
IOL powers (equivalent diopters)
+6.0 D to +27.0 D
Haptic angulation
0° (Planar)
Haptic configuration
STABLEFORCE® modified L haptic
Light filtration
UV and high-energy blue light
A-constant
118.7
Refractive index
1.55

*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).
Provided as a guideline only.

View Important Product Information for
UltraSert Pre-loaded Delivery System +

ULTRASERT 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).

ULTRASERT 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).