Fortive Corporation’s division, Advanced Sterilization Products (ASP), in collaboration with FUJIFILM Healthcare Europe GmbH, has announced that the ULTRA GI™ Cycle for the STERRAD™ 100NX Sterilizer has received CE mark approval. This regulatory approval allows the use of the ULTRA GI™ Cycle as a validated sterilization method for complex endoscopes, including FUJIFILM’s duodenoscope models ED-840T and ED-840XT, in European healthcare facilities. The CE mark approval is intended to enhance patient safety by enabling the use of hydrogen peroxide gas plasma sterilization technology for duodenoscope reprocessing.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Fortive Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 20260115179534) on January 15, 2026, and is solely responsible for the information contained therein.
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