A Clearer View: Rigid Endoscope Inspection from the Inside Out
Includes a Live Web Event on 11/19/2026 at 2:00 PM (EST)
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Objectives:
- Review the evolution of internal and external inspection tools and techniques for rigid endoscopes, comparing historical methods with current technologies available on the market.
- Examine current industry standards, professional recommendations, and manufacturers’ Instructions for Use (IFUs) related to the inspection and functionality testing of rigid endoscopes.
- Discuss FDA MAUDE reports involving near misses and adverse events associated with rigid endoscopes during surgical procedures and their potential impact on patient safety.
- Evaluate published studies and available evidence supporting the importance of both internal and external inspection of rigid endoscopes as part of routine reprocessing and quality assurance practices.
Jahan Azizi
Special Projects Manager
Healthmark, a Getinge company
Jahan Azizi, BS, CBET has spent 30 years in healthcare settings investigating and reporting problems with medical devices, his focus has always been on fixing and correcting, then moving on to the next. Jahan has several years with device manufacturing and at the Food and Drug Administration (FDA) as well. Jahan has written numerous safety reports, internal reports, presentations, and hospital policies. He has published the findings from his work, better to reach those in industries and in regulatory agencies that can effect positive changes in medical device design, maintenance, and control. Jahan has spent several years on the issue of validating and optimizing surgical instrument reprocessing methods, which has provided him with a unique skill set and knowledge. Jahan was invited to make presentations at the FDA and industry professionals at symposia of the Association for the Advancement of Medical Instrumentation (AAMI), the American Society for Testing of Materials (ASTM), the FDA's MedSun, HSPA (IAHCSMM), local societies, and Jahan is Primary Voter at several AAMI and ASTM Standard Committee(s).
Cheron Rojo
Senior Manager of Clinical Education
Healthmark, a Getinge company
Cheron Rojo is a CRCST, CIS, CER, CFER, CHL, and FCS (Fellow Central Service). He served on the PDRC (Professional Development Resource Committee) for HSPA in his career, and currently on the board of Directors for the CCSA (California Central Service Association) Chapter as president-elect.
Mr. Rojo has 30 years in the Sterile Processing arena as a has a Sterile Processing Technician, SPD Educator, an Instrument Coordinator, and a Surgical Technologist in the Surgical realm. Mr. Rojo is currently one of the Clinical Education Specialists for Healthmark Industries and has been with the company for over four years. Mr. Rojo currently resides in Las Vegas, Nevada.
He graduated with his BS in Communication and with a certificate in Marketing in April of 2021. Mr. Rojo will start working on his master’s in health administration in October as well. He is also currently on the AAMI working groups for ST79, ST91, TIR108, TIR99, and current co-chair for PB70.
Mr. Rojo has also presented to seminars/webinars across the country and internationally for numerous organizations like; APIC, SGNA, AORN, CBSPD, and HSPA, with topics relating to communication and human relations, insulation quality testing programs, and the use of effective magnification to name a few.
Mr. Rojo is a published author in the AORN Journal in the December issue in 2018 on “The Importance of Leak Testing Flexible Endoscopes “and the PROCESS magazine Jan/Feb issue in 2022 on “Inspection and Integrity Testing of Insulated Instruments: Concerns for Failure and New Guidelines for Testing.”
Cheron Rojo was named the 2018 “Educator of the Year” by the Golden West Central Service Chapter. And he also received his (FCS) Fellowship through HSPA in October of 2021 on a study regarding the issues surrounding insulation testing. Mr. Rojo is a great advocate for providing education throughout the county and globally and believes “Attitude is Everything!”