The management of many gastrointestinal diseases relies on the diagnostic and therapeutic capabilities of endoscopes. Endoscopes are considered semicritical and used in sterile body cavities. Complex endoscope design features may allow organic debris to accumulate and should be sterilized after each procedure. Although endoscopic procedures carry a minimal risk of infection, the potential transmission of exogenous infections among patients is a significant concern for patients, clinicians, healthcare facilities, endoscope manufacturers, and regulatory agencies. Hence, every patient must be considered a potential source of infection, and all endoscopes and accessory devices must be decontaminated with the same degree of rigor following every endoscopic procedure.

1 RESEARCH METHODOLOGY 

2 RESEARCH OBJECTIVES 

3 RESEARCH PROCESS 

4 SCOPE & COVERAGE、

5 REPORT ASSUMPTIONS & CAVEATS 、

6 MARKET AT A GLANCE 

7 INTRODUCTION 

8 PREMIUM INSIGHTS 

9 MARKET OPPORTUNITIES & TRENDS 

10 MARKET GROWTH ENABLERS 

11 MARKET RESTRAINTS