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SlimLine SIS (FIBERS) - ARCSA Registration e66ba8f9a3e975d767237dad9e811d4e

Access comprehensive regulatory information for SlimLine SIS (FIBERS) in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID e66ba8f9a3e975d767237dad9e811d4e 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.

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ARCSA Official Data
II
e66ba8f9a3e975d767237dad9e811d4e
SlimLine SIS (FIBERS)
ARCSA ID: e66ba8f9a3e975d767237dad9e811d4e
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Device Classification
Risk Class
II
Product Type
Invasive
Brand Name
LUMENIS
Commercial Name
Laser Delivery Systems, by Fiber Optics
Registration Information
Analysis ID
e66ba8f9a3e975d767237dad9e811d4e
Registration Date
July 26, 2018
Expiration Date
July 26, 2028
Product Use

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.

Manufacturer
City
YOKNEAM
Country
ISRAEL
Address
YOKNEAM INDUSTRIAL PARKHAKIDMA 6PO BOX NO. 240 YOKNEAM, 2069204 ISRAEL
Product Owner
Name
LUMENIS LTD
Country
ISRAEL
Authorized Representative
Address
PICHINCHA / QUITO / Iร‘AQUITO / AV. DIEGO DE ALMAGRO N31-36 AND ALPALLANA / NORTH TOWER / GALICIA BUILDING
Phone
22556496