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Clareon™ Aspheric Hydrophobic Acrylic IOL - ARCSA Registration 38635efefb5905735d0b8a75a48b8885

Access comprehensive regulatory information for Clareon™ Aspheric Hydrophobic Acrylic IOL in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 38635efefb5905735d0b8a75a48b8885 and manufactured by ALCON LABORATORIES IRELAND LTD.. The device was registered on September 17, 2021.

This page provides complete registration details including product type (Invasive), 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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III
38635efefb5905735d0b8a75a48b8885
Clareon™ Aspheric Hydrophobic Acrylic IOL
ARCSA ID: 38635efefb5905735d0b8a75a48b8885
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Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
Clareon™
Commercial Name
Intraocular lenses
Sterilization Method
ETHYLENE OXIDE
Registration Information
Analysis ID
38635efefb5905735d0b8a75a48b8885
Registration Date
September 17, 2021
Expiration Date
September 17, 2026
Creation Date
September 17, 2021
Product Use

THE CLAREON™ LIO IS DESIGNED TO BE IMPLANTED IN THE CAPSULAR SAC IN THE POSTERIOR CHAMBER OF THE EYE, REPLACING THE HUMAN LENS. THIS POSITION OF THE LENS ALLOWS THE LIO TO ACT AS A REFRACTIVE MEDIUM IN APHAKIA CORRECTION.

Manufacturer
City
CORK IRELAND
Country
IRELAND
Address
CORK BUSINESS & TECHNOLOGY PARK, MODEL FARM RD, CORK IRELAND
Product Owner
Name
ALCON LABORATORIES, INC.
Country
UNITED STATES
Authorized Representative
Address
AVENIDA AMAZONAS N37-29 AND NATIONAL UNION OF JOURNALISTS. EUROCENTER BUILDING. FLOOR 6
Phone
23933020