ESCHERICHIA COLI - ANVISA Registration 80254180482
Access comprehensive regulatory information for ESCHERICHIA COLI in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180482 and manufactured by manufacturer not specified. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until May 26, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
80254180482
25351435524202444
04930429000139
Company Information
Dates and Status
May 26, 2025
26/05/2035
09/18/2025 19:00:01
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LEGIONELLA LATEX TEST
OXOID LIMITED.
80254180276
Apr 24, 2017
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ECO F H. pylori Ag
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FASTLINE CAMPYLOBACTER Ag
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80105220132
May 08, 2023
STREPTOCOCCUS
ECO F Strep A Ag
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80954880074
Jun 11, 2018
HELICOBACTER PYLORI
FASTLINE H. PYLORI Ag
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80105220130
Apr 17, 2023