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The da Vinci Si has two separate but connected sections: The tower, which is positioned directly over the patient during surgery, contains the robot’s four arms—three that can hold a multitude of different surgical instruments, and a fourth that holds the system’s 3-D cameras.These arms are controlled by a computer that exactly replicates the movements of the operating surgeon. Gerber omega 5.0 user manual. View and Download XYZ Printing DA VINCI MINI SERIES user manual online. DA VINCI MINI SERIES 3D Printers pdf manual download. Indications for Use, United States. The Indications for Use statements below are for customers within the United States. Customers outside of the US can visit the Intended Use page or contact their local distributor or nearest Intuitive Surgical office for additional information. Da Vinci Xi ® Surgical System. The Intuitive Surgical Endoscopic Instrument Control System (da Vinci Surgical.
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Da Vinci Xi User Manual English Version
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| Intuitive sent a Field Safety Notice/Urgent Medical Device Correction letters dated March 22, 2016 by trackable mail method to their customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to 1. In addition to existing instructions for use, observe the following warning when manipulating the cardiac ablation probe, Use only the Cardiac Probe Grasper to manipulate a cardiac ablation probe. 2. Distribute a copy of this letter to all da Vinci S, Si, and Xi users at your facility. 3. Place a copy of this letter with your user manual. 4. Complete the attached Acknowledgement Form and return it to Intuitive Surgical as instructed. 5. Retain a copy of this letter and the Acknowledgement Form for your files. Intuitive Surgical will provide a user manual addendum to incorporate the warning related to this risk. For questions contact your Clinical Sales Representative or contact Intuitive Surgical Customer Service. | |||||||||||||||||||||||||||
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| Worldwide Distribution - US Nationwide in the countries Australia, Belgium, Brazil, Canada, Chile, Finland, France, Germany, Greece, Iceland, India, Israel, Italy, Netherlands, Qatar, Russia, Singapore, South Korea, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, and United Kingdom. | |||||||||||||||||||||||||||
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| 1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. | |||||||||||||||||||||||||||
| 510(K) Database | 510(K)s with Product Code = NAY and Original Applicant = INTUITIVE SURGICAL, INC. | ||||||||||||||||||||||||||