Flexible needle design for accessing lesions in anatomically challenging locations. Provides improved patient safety with reduced tissue trauma.
Manufactured by
Bagnolo San Vito (MN), Italy
Recently VIGEO Srl achieved the certification according to the new, mandatory Medical Device Regulation (MDR) 2017/745. VIGEO Srl is one of the first biopsy and breast care devices companies to receive this important certification for the future. The audit was carried out last May 2022 by three auditors from the notified body Kiwa. This is a significant achievement in both respects, bearing in mind the importance of the CE Mark in allowing easy product registration and the sale of our devices within the EU markets, as well as in all those other countries accepting the CE Mark. Receiving Medical Device Regulation certification is another important cornerstone of our Quality Management System.
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