“Reprocessing Training Webinar”

Disclosure

Training provided by Intuitive is limited to the use of Intuitive technology, instruments, and accessories. It does not replace the necessary medical training and experience required to perform procedures. Before performing any procedure using Intuitive technology, physicians are responsible for receiving sufficient training to ensure that they have the skill and experience necessary to protect the health and safety of their patients. Intuitive technology should only be used by physicians and staff who have received specific training in the use of Intuitive technology. Prior to using any training materials, refer to Intuitive Learning to ensure you are using the most up-to-date revision and that the software version of the training matches the software version installed on your system. There may be instances in which certain training content or activities listed above may not be available. For example, activities that require case history (e.g., videos or observations) may not be immediately available following a new product launch. In those cases, if you wish for additional training, please consult with your hospital and/or work with your Intuitive representative to explore alternative training activities.

For intended use and/or indications for use, risks, cautions, and warnings and full prescribing information, refer to the associated user manual(s) or visit https://manuals.intuitivesurgical.com/market.

Reprocessing

Refer to the manufacturer’s reprocessing instructions for full details regarding cleaning and disinfection of the items listed above.
It is the responsibility of the owner of the Ion endoluminal system to properly train and supervise its personnel to ensure that the Catheter, Vison Probe, and Catheter Guide are properly cleaned, disinfected, and sterilized as required by the reprocessing instructions. The Ion products should not be used in a clinical setting unless the institution has verified that these devices are properly reprocessed in accordance with the Ion system reprocessing instructions.

Europe

Da Vinci X/Xi System, Instruments, and Accessories
Medical devices, CE 2460 (and CE for select Class 1 devices and accessories), refer to Instructions for Use for further information.

Product availability

Some products, features, technologies or indications/representative uses may not be approved in all countries. Please contact your local Intuitive representative for product availability and uses in your region.

Important safety information

For important safety information, please refer to www.intuitive.com/safety For a product’s intended use and/or indications for use, risks, full cautions and warnings, please refer to the associated User Manual(s).

Da Vinci instruments and accessories

It is the responsibility of the owner of the da Vinci surgical system to properly train and supervise its personnel to ensure that the instruments and accessories are properly cleaned, disinfected, and sterilized as required by the user’s manual. Da Vinci products should not be used in a clinical setting unless the institution has verified that these products are properly processed in accordance with the da Vinci system user manual.

© 2024 Intuitive Surgical Operations, Inc. All rights reserved. Product and brand names/logos are trademarks or registered trademarks of Intuitive Surgical or their respective owner. See intuitive.com/trademarks.