0e327cfda01b5ae87eefbd5c9088cdff
OPHTHALMIC SURGICAL SYSTEM
NIDEK CO. LTD.·III·Ecuador ARCSA·Registered March 05, 2018
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
Manufacturer
- Name
- NIDEK CO. LTD.
- Country
- JAPAN
- Address
- 34-14 MAEHAMA, HIROISHI-CHO, GAMAGORI,AICHI 443-0038, JAPAN
Product owner
- Name
- NIDEK CO. LTD.
- Country
- JAPAN
Authorized representative
- Address
- OE7A N31-179 AND AV. MARIANA DE JESUS
- Phone
- 22446307
Product use
IT IS A COMBINED SYSTEM FOR USE IN CATARACT SURGERY (TYPE A) OR CATARACT SURGERY AND VITREOUS SURGERY (AP TYPE).
About this record
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.