Intraocular Lenses - ANVISA Registration 81478170022

Access comprehensive regulatory information for Intraocular Lenses in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81478170022 and manufactured by BIOTECH EUROPE MEDITECH INC LIMITED. The registration is held by BIOTECH VISION CARE OFTALMOLOGIA BRASIL LTDA with validity until Sep 27, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including JOHNSON & JOHNSON SURGICAL VISION, INC, ALCON LABORATORIES, INC, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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81478170022
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Registration Details
ANVISA Registration Number: 81478170022
Janaina dos Santos de Miranda

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Related Devices (2)

LENTE OPTIFLEX GENESIS
Risk Class III

Registration Details

81478170022

25351590235202164

19443989000136

Company Information

Ireland
PT: IRLANDA

Dates and Status

Sep 27, 2021

27/09/2031

09/18/2025 19:00:01

LENTE OPTIFLEX GENESIS
Risk Class III

Registration Details

81478170022

25351590235202164

19443989000136

Company Information

Dates and Status

Sep 27, 2021

27/09/2031

09/18/2025 19:00:01