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Moses D/L/F Fibers - ARCSA Registration 91adf4d4c580611848b078ed9160f8be

Access comprehensive regulatory information for Moses D/L/F Fibers in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID 91adf4d4c580611848b078ed9160f8be 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
91adf4d4c580611848b078ed9160f8be
Moses D/L/F Fibers
ARCSA ID: 91adf4d4c580611848b078ed9160f8be
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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
91adf4d4c580611848b078ed9160f8be
Registration Date
July 26, 2018
Expiration Date
July 26, 2028
Product Use

LUMENIS MOSES FIBERS ARE DESIGNED FOR USE WITH COMPATIBLE LASER SYSTEMS IN SURGICAL PROCEDURES INVOLVING ABLATION, VAPORIZATION, EXCISION, INCISION, OPEN SOFT TISSUE COAGULATION, LAPAROSCOPIC AND ENDOSCOPIC, FOR LITHOTRIPSY

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 / IÑAQUITO / AV. DIEGO DE ALMAGRO N31-36 AND ALPALLANA / NORTH TOWER / GALICIA BUILDING
Phone
22556496