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Laserlith i-dust - ARCSA Registration 718b07ad621c2a5bddaa097e51739de4

Access comprehensive regulatory information for Laserlith i-dust in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 718b07ad621c2a5bddaa097e51739de4 and manufactured by QUANTA SYSTEM S.P.A. The device was registered on April 30, 2020.

This page provides complete registration details including product type (Active), 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
III
718b07ad621c2a5bddaa097e51739de4
Laserlith i-dust
ARCSA ID: 718b07ad621c2a5bddaa097e51739de4
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Pricing
Device Classification
Risk Class
III
Product Type
Active
Brand Name
HOW MUCH
Commercial Name
Litotriptores
Registration Information
Analysis ID
718b07ad621c2a5bddaa097e51739de4
Registration Date
April 30, 2020
Expiration Date
April 30, 2025
Product Use

UD: LASERLITH I-DUST IS INDICATED FOR USE IN GENERAL SURGICAL APPLICATIONS FOR: INCISION, EXCISION, VAPORIZATION, ABLATION, HEMOSTASIS OR COAGULATION OF SOFT TISSUE IN CONTACT OR NOT CONTACT MODE (WITH A COMPATIBLE LASER MARKETED FOR USE IN THE DESIRED APPLICATION), IT IS USED IN GENERAL SURGERY.

Manufacturer
Country
ITALY
Address
AGNELLO, 5-20121 MILANO (MI), ITALY
Product Owner
Name
EDAP TMS FRANCE
Country
FRENCH
Authorized Representative
Address
PICHINCHA / QUITO / Iร‘AQUITO / AV. DIEGO DE ALMAGRO N31-36 AND ALPALLANA / NORTH TOWER / GALICIA BUILDING
Phone
22556496