Drivers and fleets using the PremierRide Logs, DSG Elogs, and State Elogs ELD devices should revert to paper and find ...
Great Britain is entering a new era of MedTech regulation, with major pre-market changes expected that are designed to ...
In June 2025, the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024 came ...
The new facility accelerates catheter design with rapid prototyping, testing capabilities, and university research ...
Minneapolis-based Imricor Medical Systems said it won 510(k) clearance from the FDA for its Vision-MR Diagnostic Catheter.
The U.K. Medicines and Health Care Products Regulatory Agency provided an update of its guidance for clinical investigations ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results