Recall of Medtronic embolization devices classified as most serious by USFDA Ruchika Sharma20 March 2025 4:45 PM ISTMedtronic's recall of embolization device has been classified most serious by the U.S. Food and Drug Administration (USFDA), citing potential risks of...
JnJ MedTech gets clearance for MONARCH QUEST for enhanced Robotic-Assisted Bronchoscopy Ruchika Sharma14 March 2025 10:00 AM ISTSanta Clara: Johnson & Johnson MedTech has announced U.S. 510(k) regulatory clearance for MONARCH QUEST, the latest advancement in MONARCH...
Parliamentary Panel Slams CDSCO for Slow Drug Approvals, Calls for Conditional Licensing in 45 Days Farhat Nasim13 March 2025 7:17 PM ISTThe delays and frequent queries raised by CDSCO have become a major obstacle for applicants, particularly startups and entrepreneurs.
Johnson and Johnson Wins Rs 3.34 Crore Lawsuit Against Fake SURGICEL, ETHICON Sellers Farhat Nasim12 March 2025 9:16 PM ISTNew Delhi: The Delhi High Court has ruled in favor of Johnson & Johnson (J&J), awarding the company Rs 3.34 crore in damages against Medserve...
Shockwave Medical unveil Forward Intravascular Lithotripsy Platform in US Ruchika Sharma6 March 2025 3:42 PM ISTSanta Clara: Shockwave Medical, Inc., part of Johnson & Johnson MedTech has announced the U.S. launch of its Shockwave Javelin Peripheral IVL...
Siemens sells 2 percent stake in Siemens Healthineers, raises around USD 1.5 billion Ruchika Sharma20 Feb 2025 3:27 PM ISTSiemens, a German engineering giant has successfully raised approximately 1.45 billion euros ($1.5 billion) by selling a stake in its healthcare...
JnJ to resume US VARIPULSE cases Ruchika Sharma20 Feb 2025 9:30 AM ISTNew Brunswick: Johnson & Johnson will resume the limited market release of VARIPULSE in the United States after a comprehensive...
Johnson & Johnson MedTech launches CEREGLIDE 92 Catheter System for Acute ischemic stroke Ruchika Sharma13 Feb 2025 4:54 PM ISTIrvine: Johnson & Johnson MedTech, an emerging leader in neurovascular care, has announced the launch of the CEREGLIDE 92 Catheter System, a...
EMA establishes regular procedure for scientific advice on certain high-risk medical devices Ruchika Sharma11 Feb 2025 3:30 PM ISTEuropean Medicines Agency (EMA), in close collaboration with the European Commission, has established a standard procedure for manufacturers of...
Union Budget 2025 Disappoints Medical Devices Industry, No Relief for Import Dependency: AiMed Farhat Nasim1 Feb 2025 3:05 PM ISTNew Delhi: The Union Budget 2025 has laid out a strong macro-economic and policy direction, but it has left the medical devices industry disheartened...
Shalby receives USFDA clearance for knee replacement device Ruchika Sharma21 Jan 2025 10:00 AM ISTShalby Advanced Technologies Inc., USA, a step down subsidiary of the Company has received U.S. Food and Drug Administration (FDA) 510(k) Premarket ...
Government Bans Import of Refurbished Medical Devices Farhat Nasim17 Jan 2025 6:44 PM ISTNew Delhi: The Central Drugs Standard Control Organisation (CDSCO) has issued a directive to halt the import of refurbished medical devices, citing...
