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BioWorld - Tuesday, January 20, 2026
Home » Topics » Europe, BioWorld MedTech

Europe, BioWorld MedTech
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Toku Clair platform

Toku receives CE, UKCA marks for cardio disease AI risk evaluation tool

Feb. 8, 2024
By Shani Alexander
Toku Inc. recently obtained CE and UKCA marks for its artificial intelligence (AI) technology, Clair, which evaluates the risk of cardiovascular disease (CVD) using retinal images captured during an eye exam.
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neuromodulation urinary tract

Improved neuromodulation technique for treating urinary tract dysfunction

Feb. 8, 2024
By Simon Kerton
The Belgian academic Stefan De Wachter is seeking patent protection for methods of ensuring pelvic health and treating a disease or disorder characterized by a dysfunctional autonomic nervous system using neuromodulation and applying a burst stimulation pattern of electric pulses of high frequencies from electrodes located in the proximity of the sacral plexus and/or pelvic plexus.
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Tinted Euro symbol

Theryq, Gustave Roussy given €38M for cancer radiotherapy

Feb. 5, 2024
By Shani Alexander
Theryq SAS and Gustave Roussy, a European center for cancer research, were given €38 million (US$40.1 million) in funding by Bpifrance, the French public sector investment bank, to further develop Flashdeep, a flash radiotherapy device that uses extremely high energy electron (VHEE) radiation to treat cancers that are resistant to traditional treatments.
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EU flags

EU nudges Artificial Intelligence Act further along

Feb. 5, 2024
By Mark McCarty
The European Union (EU) is steadily making progress on the Artificial Intelligence Act (AI Act), landmark legislation that will affect AI not just for medical uses, but for all uses across the EU economy.
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MHRA logo

UK’s MHRA relaxes restrictions on use of paclitaxel devices in PAD

Feb. 5, 2024
The controversy over the use of paclitaxel (PTX) in devices used to treat peripheral artery disease (PAD) has taken roughly half a decade to unwind as regulatory agencies across the globe stand down their restrictions on the use of these devices.
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WaveForm cgm

Trinity transforming into CGM player with $12.5M acquisition, Bayer partnership

Feb. 1, 2024
By Shani Alexander
Trinity Biotech plc. paid $12.5 million to acquire Waveform Technologies Inc.’s biosensor and continuous glucose monitoring (CGM) assets. It also formed a partnership with Bayer AG to launch a CGM biosensor in China and India. These moves are part of Trinity’s transformation strategy to become a leading player in wearable biosensor technology.
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Opto Biosys brain sensor
Patents

Opto Biosystems develops sensors for monitoring brain activity

Jan. 29, 2024
By Simon Kerton
In its first patenting, Cambridge, U.K.-based Opto Biosystems Ltd. is seeking protection for implantable sensors that may be used in systems to measure chemical, biological, or electrical signals in the central and/or peripheral nervous systems.
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Brain with stroke illustration

UK’s NICE easing into artificial intelligence for stroke

Jan. 26, 2024
By Mark McCarty
To date, developers of digital health technologies have had little luck with coverage and reimbursement, but the picture is slowly improving. The U.K.’s National Institute for Health and Care Excellence (NICE) has endorsed two artificial intelligence (AI) algorithms for diagnosis of stroke, although this is limited to an evidence generation framework that puts the sponsors on the hook for generating the data that will allow unlimited use in the U.K.’s trusts.
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Allurion Balloon

Allurion’s swallowable gastric balloon introduced into the UK NHS

Jan. 25, 2024
By Shani Alexander
A U.K. national health service (NHS) hospital has begun offering Allurion Technologies Inc.’s swallowable gastric balloon to patients struggling to lose weight for surgery. The move is a boon for the company amid rising competition in the weight loss market from GLP-1 agonists.
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EU flags

European Commission provides another delay in IVDR compliance deadlines

Jan. 24, 2024
By Mark McCarty
The European Commission (EC) has proposed another delay in the compliance deadlines for the In Vitro Diagnostic Regulation (IVDR) that eases the existing timelines by roughly two and a half years. The news was welcomed by Medtech Europe, which nonetheless pressed the EC and others to patch up some of the issues that led to the new extensions in the first place.
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