DEVICE FOR DIAGNOSIS - ANVISA Registration 80443070020

Access comprehensive regulatory information for DEVICE FOR DIAGNOSIS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80443070020 and manufactured by LEEDSAY S/A. The registration is held by LEEDSAY S/A with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MADHU INSTRUMENTS PVT. LTD, MIRO VERBANDSTOFFE GMBH, 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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80443070020
Registration Details
ANVISA Registration Number: 80443070020
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

OPHTHAL-FLUOR ® EYE DROPS
Risk Class I

Registration Details

80443070020

25351104104202176

08116472000116

Company Information

LEEDSAY S/A
Brazil
PT: BRASIL

Dates and Status

Mar 04, 2021

VIGENTE

09/18/2025 19:00:01