OPHTHALMIC YAG LASER SYSTEM
- Risk class
- III
- Product type
- Active
- Brand name
- NIDEK
- Commercial name
- Diode Lasers for Ophthalmology
- Sterilization method
- NON-STERILE
- Analysis ID
- a9cb79eee01ab1f5552b42f75329a63b
- Registration date
- December 31, 2018
- Expiration date
- December 31, 2023
- Creation date
- February 01, 2019
- Name
- NIDEK CO. LTD.
- City
- GAMAGORI CITY
- Country
- JAPAN
- Address
- 34-14 MAEHAMA, HIROISHI-CHO, GAMAGORI,AICHI 443-0038, JAPAN
- Name
- NIDEK CO. LTD.
- Country
- JAPAN
- Address
- CALLE OE7A N31-179 Y AV. MARIANA DE JESUS
- Phone
- 2446307
IT IS TO PERFORM POSTERIOR CAPSULOTOMY, PUPILLARY MEMBRANECTOMY AND IRIDOTOMY (HOLE IN THE IRIS) FOR PHAKIC, APHAKIC OR PSEUDOPHACHIC PATIENTS.
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.