UltraSert® Preloaded Delivery System
UltraSert® Preloaded Delivery System
Gain consistency in IOL delivery, injection control and enhance the efficiency of your OR1
Consistency in IOL Delivery for Reduced Intraoperative Variability1-3
*Observations during porcine cadaver eye study to evaluate consistency of leading haptic configuration using permissible delivery configurations identified in the UltraSert® Directions for Use. Study conducted using UltraSert® optimized with 3 mm (extended) tip and inner lumen adjustment (n=184-187). VISCOAT® OVD was used at operating room temperatures (approximately 65 to 73 degrees).
UltraSert® helps minimise wound stretch compared to other delivery devices1,3,5
*Before IOL implantation, corneal incisions were made (2.2 mm knife for IOL implantation with UltraSert®, iTxx and iSxxx 250/251; 2.4 mm knife for IOL implantation with Monarch® III) and initial incision size was measured and documented. Post-IOL implantation incision size was measured and documented via the same process. UltraSert® (n=19) presented with a significantly smaller mean corneal incision size after IOL implantation compared with iTxx (n=26), iSxx 250/251 (n=26) and Monarch® III (n=28). For each, p < 0.001. Testing completed with first-generation UltraSert® (2 mm nozzle tip).
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Enhanced Injection Control for Smooth IOL Delivery1
UltraSert® features the spring-controlled TensionGlide™ Plunger for smooth IOL deployment.1,6
TensionGlide™ maintains injection force stability6
TensionGlide™ mitigates the risk of sudden forceful IOL ejection, offering the ideal amount of resistance6,7
Efficiency and Enhanced Patient Throughput8,9
UltraSert® helps streamline patient throughput with a low average preparation time.8,9
UltraSert® is ready to implant in 3 simple steps10
UltraSert® is Preloaded with AcrySof® IQ IOL10
The trusted IOL that gives you complete confidence
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Clinical Studies
Technical Specifications10
Instructions for Use (IFU)
For a full list of indications, contraindications and warnings, please visit ifu.alcon.com and refer to the relevant product’s instructions for use.
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References:
1. Alcon Data on File, REF-02270, 2015.
2. Wang L, Wolfe P, Chernosky A, Paliwal S, Tjia K, Lane S. In vitro delivery performance assessment of a new preloaded intraocular lens delivery system. J Cataract Refract Surg. 2016;42(12):1814–1820.
3. Mendicute J, Amzallag T, Wang L, Martinez AA. Comparison of incision size and intraocular lens performance after implantation with three preloaded systems and one manual delivery system. Clin Ophthalmol. 2018;12:1495–1503.
4. Alcon Data on File, REF-04197, 2019.
5. Amzallag T, Mendicute J, Martinez A. Multicenter clinical assessment of a pre-loaded IOL delivery system. Paper presented at ASCRS Congress; May 5-9, 2017; Los Angeles, CA.
6. Alcon Data on File, REF-02260, 2016.
7. Alcon Data on File, REF-07653, 2015.
8. Nanavaty MA, Kubrak-Kisza M. Evaluation of preloaded intraocular lens injection systems: Ex vivo study. J Cataract Refract Surg. 2017 Apr;43(4):558-563.
9. Mendicute J, Pablo L, Vélasque L, Martinez A, Asmar J, Schweitzer C. Multicenter evaluation of time, operational and economic efficiencies of a new pre-loaded intraocular lens delivery system vs. manual intraocular lens delivery. Clin Ophthalmol. 2021:15;591-599.
10. AcrySof IQ with UltraSert Product Information, 2017.
Please refer to the relevant product direction for use for list of indications, contraindications and warnings.
AcrySof IQ UltraSert GC22421516017
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