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Medical Devices News - Page 3

JnJ seeks USFDA approval of Stelara for pediatric Crohns disease

Johnson and Johnson Wins Rs 3.34 Crore Lawsuit Against Fake SURGICEL, ETHICON Sellers

Farhat Nasim12 March 2025 9:16 PM IST
New 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

Shockwave Medical unveil Forward Intravascular Lithotripsy Platform in US

Ruchika Sharma6 March 2025 3:42 PM IST
Santa 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

Siemens sells 2 percent stake in Siemens Healthineers, raises around USD 1.5 billion

Ruchika Sharma20 Feb 2025 3:27 PM IST
Siemens, a German engineering giant has successfully raised approximately 1.45 billion euros ($1.5 billion) by selling a stake in its healthcare...
Imbruvica gets positive EMA Committee opinion for untreated mantle cell lymphoma eligible for Stem Cell Transplant: Janssen-Cilag International

JnJ to resume US VARIPULSE cases

Ruchika Sharma20 Feb 2025 9:30 AM IST
New Brunswick: Johnson & Johnson will resume the limited market release of VARIPULSE in the United States after a comprehensive...
JnJ seeks USFDA approval of Stelara for pediatric Crohns disease

Johnson & Johnson MedTech launches CEREGLIDE 92 Catheter System for Acute ischemic stroke

Ruchika Sharma13 Feb 2025 4:54 PM IST
Irvine: Johnson & Johnson MedTech, an emerging leader in neurovascular care, has announced the launch of the CEREGLIDE 92 Catheter System, a...
Eye condition NAION is a very rare side effect of semaglutide: EMA safety committee

EMA establishes regular procedure for scientific advice on certain high-risk medical devices

Ruchika Sharma11 Feb 2025 3:30 PM IST
European Medicines Agency (EMA), in close collaboration with the European Commission, has established a standard procedure for manufacturers of...
Himachal to develop medical device park independently

Union Budget 2025 Disappoints Medical Devices Industry, No Relief for Import Dependency: AiMed

Farhat Nasim1 Feb 2025 3:05 PM IST
New Delhi: The Union Budget 2025 has laid out a strong macro-economic and policy direction, but it has left the medical devices industry disheartened...
USFDA

Shalby receives USFDA clearance for knee replacement device

Ruchika Sharma21 Jan 2025 10:00 AM IST
Shalby Advanced Technologies Inc., USA, a step down subsidiary of the Company has received U.S. Food and Drug Administration (FDA) 510(k) Premarket ...
Adverse drug reactions from normal saline: Punjab imposes 3-year ban on Captab Biotech

Government Bans Import of Refurbished Medical Devices

Farhat Nasim17 Jan 2025 6:44 PM IST
New Delhi: The Central Drugs Standard Control Organisation (CDSCO) has issued a directive to halt the import of refurbished medical devices, citing...
CDSCO grants license to Time Medical International Ventures (India) for manufacturing, distributing MRI systems

CDSCO grants license to Time Medical International Ventures (India) for manufacturing, distributing MRI systems

Ruchika Sharma15 Jan 2025 12:30 PM IST
Vishakapatnam: Time Medical International Ventures (India) Private Limited, a Wholly Owned Subsidiary of Fischer Medical Ventures Limited, a Make...
Dr Reddys Labs, Alvotech ink pact to codevelop biosimilar candidate to Keytruda

CDSCO Panel approves Dr Reddys proposal to increase patients from 241 to 265 in India for anticancer drug Nivolumab study

Dr. Divya Colin12 Jan 2025 5:45 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has granted approval to the drug...
Indias Medical Device Exports to US Hit by 26% Reciprocal Tariff: AiMeD Raises Concerns

CDSCO Releases Draft: 1,178 Medical Devices to be Reclassified into 4 Categories, AiMeD Welcomes Move

Farhat Nasim11 Jan 2025 6:09 PM IST
However, AiMeD urged regular meetings with stakeholders to clarify compliance and align Medical Device Rules interpretations across regulators.
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