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Instrument Kit - ANVISA Registration 80136060359

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80136060359 and manufactured by BAUSCH & LOMB INC. The registration is held by BL INDÚSTRIA OTICA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.A, 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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80136060359
Registration Details
ANVISA Registration Number: 80136060359
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Device Details

Kit Instrumental Adaptive Fluidics STANDARD PACK
Risk Class II

Registration Details

80136060359

25351682642201800

27011022000103

Company Information

BAUSCH & LOMB INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 03, 2018

VIGENTE

09/18/2025 19:00:01