Preclinical Study
Further Validating the Robotic Microsurgery Platform through Preclinical Studies on Rat Femoral Artery and Vein
Journal of Reconstructive Microsurgery
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The Symani Surgical System is authorized for use in the U.S. by the FDA and is a CE marked medical device. Symani is manufactured in Pisa, Italy.
Clinical indications vary by geography. Refer to global indications for more information.
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