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Elegant Technology for Renal Denervation Treatment. In preclinical trials, the company’s flagship TIVUS system has shown excellent results. Cardiosonic Received CE Mark for Its TIVUS Ablative Catheter Device. Cardiosonic announces completion of the TIVUS I Trial and the start of the TIVUS II Trial. Cardiosonic Announces Initial Enrollment in the TIVUS I Trial. Cardiosonic Closes $6.1 Million in phased Series B Financing. The TIVUS system is approved for sale in markets regulated by the CE mark.

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cardiosonic - Home | cardiosonic.co.il Reviews

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Elegant Technology for Renal Denervation Treatment. In preclinical trials, the company’s flagship TIVUS system has shown excellent results. Cardiosonic Received CE Mark for Its TIVUS Ablative Catheter Device. Cardiosonic announces completion of the TIVUS I Trial and the start of the TIVUS II Trial. Cardiosonic Announces Initial Enrollment in the TIVUS I Trial. Cardiosonic Closes $6.1 Million in phased Series B Financing. The TIVUS system is approved for sale in markets regulated by the CE mark.

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4 procedure

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6 system components

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cardiosonic - Home | cardiosonic.co.il Reviews

https://cardiosonic.co.il

Elegant Technology for Renal Denervation Treatment. In preclinical trials, the company’s flagship TIVUS system has shown excellent results. Cardiosonic Received CE Mark for Its TIVUS Ablative Catheter Device. Cardiosonic announces completion of the TIVUS I Trial and the start of the TIVUS II Trial. Cardiosonic Announces Initial Enrollment in the TIVUS I Trial. Cardiosonic Closes $6.1 Million in phased Series B Financing. The TIVUS system is approved for sale in markets regulated by the CE mark.

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cardiosonic.co.il

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cardiosonic - Management

http://www.cardiosonic.co.il/company/management

Benny Dilmoney, CEO. Benny joined Cardiosonic with its establishment in 2009, and brings over a decade R&D and executive management experience in the medical device industry to the company. He holds a B.Sc. in Mechanical Engineering. Co-founder and Current CTO of Cardiosonic LTD. MSc Biomed. Eng. , B.Sc. Mech. Eng. ; Technion - Israel Institute of Technology. Tami Abudi, VP Clinical and Regulatory Affairs. Yehuda Zadok, VP R&D. Yehuda joined Cardiosonic in early 2011, after few roles as project manager, ...

2

cardiosonic - Procedure

http://www.cardiosonic.co.il/tivus/procedure

The TIVUS System was developed to perform safe, reliable and highly reproducible transluminal renal nerve ablation using non-focused ultrasound technology. In summary, the unique TIVUS technology is used for effectively reducing BP, concomitantly with protecting the integrity of the arterial wall and reducing the risk of stenosis. The TIVUS system is approved for sale in markets regulated by the CE mark. The TIVUS system is not approved for sale in the USA.

3

cardiosonic - Clinical

http://www.cardiosonic.co.il/clinical

FIM study completed successful enrolment of 15 patient plus an additional 3 patients under compassionate use due to impaired renal function and prior stent. Totally Number of Successfully Treated patients: 18. Confirmed Safety: No device-related complications. BP reduction consistent with other therapies. Reported to be less painful compared with RF technology (substantially less analgesics, site feedback). Inherent characteristics of ultrasound allows use of less contrast. In-stent treatment is feasible.

4

cardiosonic - System Components

http://www.cardiosonic.co.il/tivus/system-components

The TIVUS system consists of two main components: a TIVUS catheter and a control console. Two TIVUS catheter types are developed by Cardiosonic ltd. The Unidirectional TIVUS catheter is designed for standard transcatheter intervention- compatible with industry-standard 8 Fr guiding catheter and 0.014' guide wire. The unique treatment head of the catheter is featured with inherent distancing mechanism and multidirectional ultrasonic transducers, for simultaneous ultrasonic energy delivery in several circu...

5

cardiosonic - News

http://www.cardiosonic.co.il/news

Cardiosonic Received CE Mark for Its TIVUS Ablative Catheter Device. Cardiosonic announces completion of the TIVUS I Trial and the start of the TIVUS II Trial. Cardiosonic Announces Initial Enrollment in the TIVUS I Trial. Cardiosonic Closes $6.1 Million in phased Series B Financing. The TIVUS system is approved for sale in markets regulated by the CE mark. The TIVUS system is not approved for sale in the USA.

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cardiosonic - Home

Elegant Technology for Renal Denervation Treatment. In preclinical trials, the company’s flagship TIVUS system has shown excellent results. Cardiosonic Received CE Mark for Its TIVUS Ablative Catheter Device. Cardiosonic announces completion of the TIVUS I Trial and the start of the TIVUS II Trial. Cardiosonic Announces Initial Enrollment in the TIVUS I Trial. Cardiosonic Closes $6.1 Million in phased Series B Financing. The TIVUS system is approved for sale in markets regulated by the CE mark.

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