Endoscopy Video Processor Market Restraint
Product recalls due to failures in meeting regulatory standards as per U.S. Food and Drug Administration (USFDA) is expected to restrain growth of the endoscopy video processor market.
For instance, in October 2017, USFDA recalled Fujifilm Medical Systems U.S.A., Inc.'s product- Ultrasonic Endoscope Model Number ED-530XT (a duodenoscope, designed for visualizing the duodenum and the upper digestive track) for updating labels and design and correcting past incidence of infections.
Endoscopy Video Processor Market Report Snapshots
Joining thousands of companies around the world committed to making the Excellent Business Solutions.
View All Our Clients