France
Intelligence de marché des dispositifs médicaux pour France. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
A study comparing hemoglobin measurements from the Masimo SpHb™ device and clinical laboratory results has been completed.
The EPBONF study evaluates a surgical template for guiding BONF surgery in treating craniostenosis.
The Sub Epidermal Moisture Scanner is a non-invasive device for detecting fluid in the hypodermis to prevent pressure injuries.
A new computerized device for Mirror Therapy aims to enhance compliance and efficiency in hemiplegic rehabilitation.
The IKORUS device was evaluated for feasibility in major abdominal surgery patients with advanced hemodynamic monitoring.
The REAL-MOOV-LUNG study evaluated the impact of Moovcare® Lung on lung cancer patient care management over 24 months.
A device for proprioceptive stimulation aims to prevent muscle atrophy during post-operative bed confinement.
The Sunrise® device offers a new integrated solution for diagnosing Sleep Apnea Syndrome, improving on traditional PSG methods.
A study is recruiting to collect clinical data for a breath-based glucose measurement device developed by BOYDSense.
The SWALL EHPAD study evaluates the acceptability of the Swallis DSA™ device for swallowing assessment in nursing homes.
A study is recruiting to evaluate a universal surgical device for mandibular reconstruction using fibula free flap.
The study evaluated the efficacy of Remedee One for managing peripheral osteoarthritis pain alongside conventional treatment.
RGn600, a non-invasive device, is being tested for efficacy in mild-to-moderate Alzheimer's disease treatment.
A validation study confirmed the HWA09 watch's software for detecting atrial fibrillation against reference ECG.
The DERMAPOL device, designed for skin lesion diagnosis, has been terminated after its clinical trial in France.
The Modjaw® device reliably records condylar movements in oral rehabilitation, aiding prosthetic design.
The THALES-EVAQUAL study evaluated the C-ARM ARCO FP-Rk521S for image quality in surgical applications.
A completed study evaluated the safety of the Smart-TO device for fetoscopic endoluminal tracheal occlusion in fetuses.
A clinical study completed on the BOYDSense® breath glucose monitoring system for type 2 diabetes patients.
The FH ORTHO SAS Knee Observatory aims to collect real-life clinical data for knee arthroplasty devices under PMCF regulations.