Xpeeda D/S/L Fiber - ARCSA Registration d2c8cdc68ea5dd8f0e84a856d84da1c9
Access comprehensive regulatory information for Xpeeda D/S/L Fiber in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID d2c8cdc68ea5dd8f0e84a856d84da1c9 and manufactured by LUMENIS LTD. The device was registered on July 26, 2018.
This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
THE SINGLE-USE SLIMLINE (SIS) GI FIBER LASER INTELLIGENT IDENTIFICATION SYSTEM IS DESIGNED AND MANUFACTURED BY LUMENIS AND WILL BE USED WITH THE VERSAPULSE FAMILY OF HOLMIUM LASERS. SLIMLINE LASER FIBER IS DESIGNED FOR THE TREATMENT OF GALLSTONES AND BENIGN AND MALIGNANT NEOPLASMS.