CRYPTOCOCCUS NEOFORMANS - ANVISA Registration 80105220179

Access comprehensive regulatory information for CRYPTOCOCCUS NEOFORMANS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80105220179 and manufactured by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA. The registration is held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA with validity until Mar 11, 2034.

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 REMEL INC, BIOSYNEX S.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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80105220179
Registration Details
ANVISA Registration Number: 80105220179
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FASTLINE CRYPTOCOCCUS Ag
Risk Class III

Registration Details

80105220179

25351795550202348

04299232000143

Dates and Status

Mar 11, 2024

11/03/2034

09/18/2025 19:00:01