France
Intelligence de marché des dispositifs médicaux pour France. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
The BePoW device has completed evaluation for reliable wheelchair sitting posture measurement without MCPAA scale.
A portable medical device for breast cancer screening is being assessed in an active study.
A completed study in France assessed a probiotic medical device's effect on abdominal pain in IBS patients.
A clinical trial assesses the safety and efficacy of a RegenMatrix device combining PRP and HA for knee osteoarthritis.
A study completed by University Hospital, Rouen, evaluated the Herbst device for treating moderate obstructive sleep apnea.
A study evaluated glycemic control in in-patients using the Accu-Chek Inform system across three departments.
BIOMERIEUX SA has registered a medical device with product code JJH in the FDA database.
A multicenter trial is assessing the safety of the ProTool device for glioma tissue imprinting.
The study evaluates the cost-effectiveness of the Alfapump® device for refractory ascites in cirrhotic patients.
Exotec Dentaire's SEQUENCEUR RC TITANE BLEU CORPORIS is classified as Class IIa medical device.
M&A and divestitures are reshaping MedTech strategies, emphasizing market access for sustained growth and valuation.
The terminated study assessed fluorescence imaging techniques for prostate chips in transurethral resections.
A study evaluated automated chest compression devices for improving blood pressure in cardiac arrest patients.
The pilot clinical investigation on HEMOBLAST™ assesses SBSS reliability and initial safety data in surgeries.
A clinical study is recruiting to validate the Withings BPM Pro 2 for blood pressure measurement in pregnancy.
Thales AVS France SAS has registered two medical devices with the FDA under product code JAA.
A new device using millimeter band radiation aims to reduce postoperative morphine use in pain management.
The study evaluated the Mallinckrodt electronic device for continuous tracheal cuff pressure control to reduce risks in critically ill patients.
A study on preventing mucositis and peri-implantitis using an air-polishing device has been withdrawn.
A completed study evaluated a medical device's efficacy and tolerance for treating wounds in healthy subjects.