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LASER PHOTOCOAGULATOR - ARCSA Registration 861b33838f889886873e15822e359bb8

Access comprehensive regulatory information for LASER PHOTOCOAGULATOR in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 861b33838f889886873e15822e359bb8 and manufactured by NIDEK CO. LTD.. The device was registered on November 06, 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
861b33838f889886873e15822e359bb8
LASER PHOTOCOAGULATOR
ARCSA ID: 861b33838f889886873e15822e359bb8
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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
861b33838f889886873e15822e359bb8
Registration Date
November 06, 2018
Expiration Date
November 06, 2023
Creation Date
June 11, 2018
Product Use

TO BE USED IN OPHTHALMIC SURGERY PROCEDURES, INCLUDING RETINAL AND MACULAR PHOTOCOAGULATION, IRIDOTOMY AND TRABECULOPLASTY.

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