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OPHTHALMIC YAG LASER SYSTEM - ARCSA Registration a9cb79eee01ab1f5552b42f75329a63b

Access comprehensive regulatory information for OPHTHALMIC YAG LASER SYSTEM in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID a9cb79eee01ab1f5552b42f75329a63b and manufactured by NIDEK CO. LTD.. The device was registered on December 31, 2018.

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
a9cb79eee01ab1f5552b42f75329a63b
OPHTHALMIC YAG LASER SYSTEM
ARCSA ID: a9cb79eee01ab1f5552b42f75329a63b
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Device Classification
Risk Class
III
Product Type
Active
Brand Name
NIDEK
Commercial Name
Diode Lasers for Ophthalmology
Sterilization Method
NON-STERILE
Registration Information
Analysis ID
a9cb79eee01ab1f5552b42f75329a63b
Registration Date
December 31, 2018
Expiration Date
December 31, 2023
Creation Date
February 01, 2019
Product Use

IT IS TO PERFORM POSTERIOR CAPSULOTOMY, PUPILLARY MEMBRANECTOMY AND IRIDOTOMY (HOLE IN THE IRIS) FOR PHAKIC, APHAKIC OR PSEUDOPHACHIC PATIENTS.

Manufacturer
City
GAMAGORI CITY
Country
JAPAN
Address
34-14 MAEHAMA, HIROISHI-CHO, GAMAGORI,AICHI 443-0038, JAPAN
Product Owner
Name
NIDEK CO. LTD.
Country
JAPAN
Authorized Representative
Address
CALLE OE7A N31-179 Y AV. MARIANA DE JESUS
Phone
2446307