LifeTech and Medtronic Further Strategic Collaboration

To Open New Chapter of Domestically-Made MRI-Conditional Pacemakers

LifeTech Scientific Corporation (LifeTech, 01302.HK) announced that it has extended its agreements with Medtronic to further the strategic collaboration on the “HeartTone™ domestic pacemaker project” and to start the collaboration on domestically-made MRI-conditional pacemakers. Together with MRI-conditional leads, these products will address growing MRI-related therapeutic needs in China.

The agreements also include the extension of the partnership on the “HeartTone™ domestic pacemaker project” to 2028. Similar to its collaboration on the first generation of HeartTone™ pacemakers, Medtronic will provide a series of specialized technical consulting services for the MRI-conditional products project.

Magnetic Resonance Imaging (MRI) is recognized as the “gold standard” in diagnosis of tumors, neurological diseases, and chondropathy. However, strong magnetic field environment during an MRI scan can have adverse effects on non-MRI conditional pacemakers, which may cause serious conditions such as myocardial damage and arrhythmias in patients. Therefore, patients with non-MRI conditional pacemaker have long been prohibited from MRI scan.

According to statistics, there is over a million of patients needing a pacemaker in China. The demand for MRI scan from patients with bradycardia is increasing as society ages. MRI-conditional pacemakers can meet the demand for MRI scans of patients with implanted pacemaker. Meanwhile, implanting MRI-conditional cardiovascular implantable electronic devices (CIED) has been upgraded to Class I recommendation according to the 2021 European Society of Cardiology (ESC) Guidelines on cardiac pacing and cardiac resynchronization therapy. However, only imported MRI-conditional pacemakers are currently available in China. The collaboration between LifeTech and Medtronic will change this landscape once the MRI-conditional products are approved by NMPA.

“This collaboration between LifeTech and Medtronic represents a remarkable step forward in localizing pacing products for China market”, said Mr. Xie Yuehui, Chairman and CEO of LifeTech. “With Medtronic’s world-leading technology and LifeTech’s expertise in China market, plus a long-term collaboration with Medtronic in pacing products for China market, we are pretty confident and are expecting LifeTech MRI-conditional products to soon become a choice of selection by China patients with internationally advanced technology and superior quality, thereby making advanced domestic cardiac pacing therapies more accessible.”

“Medtronic and LifeTech have been partnering for nearly a decade, and in that time, we have successfully expanded access to pacemakers in China, via the HeartTone pacemaker,” said Mike Marinaro, president of Medtronic Cardiac Rhythm Management. “We are pleased to extend our collaboration by adding the development of domestically made MRI-conditional pacemakers for the Chinese market.”

LifeTech began its strategic relationship with Medtronic, Inc. in pacemaker product development since 2014. In December 2017, LifeTech’s HeartTone™ brand implantable cardiac pacemakers were successfully launched in the Chinese market with accompanying leads and programmers, providing a complete resolution for China patients. This latest collaboration will further meet the fast-growing demand for MRI-conditional cardiac pacing therapies in China, benefiting patients who suffer from bradycardia.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”