OPHTHALMIC SURGICAL SYSTEM - ARCSA Registration 0e327cfda01b5ae87eefbd5c9088cdff
Access comprehensive regulatory information for OPHTHALMIC SURGICAL SYSTEM in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 0e327cfda01b5ae87eefbd5c9088cdff and manufactured by NIDEK CO. LTD.. The device was registered on March 05, 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
0e327cfda01b5ae87eefbd5c9088cdff
OPHTHALMIC SURGICAL SYSTEM
ARCSA ID: 0e327cfda01b5ae87eefbd5c9088cdff
Device Classification
Risk Class
III
Product Type
Active
Brand Name
NIDEK
Commercial Name
Units for Cataract Extraction, by Phacoemulsification
Sterilization Method
NON-STERILE
Registration Information
Analysis ID
0e327cfda01b5ae87eefbd5c9088cdff
Registration Date
March 05, 2018
Expiration Date
March 05, 2023
Creation Date
March 16, 2021
Product Use
IT IS A COMBINED SYSTEM FOR USE IN CATARACT SURGERY (TYPE A) OR CATARACT SURGERY AND VITREOUS SURGERY (AP TYPE).
Manufacturer
Product Owner
Name
NIDEK CO. LTD.
Country
JAPAN
Authorized Representative
Address
OE7A N31-179 AND AV. MARIANA DE JESUS
Phone
22446307