CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE) - ANVISA Registration 81325990322

Access comprehensive regulatory information for CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81325990322 and manufactured by HANGZHOU ALLTEST BIOTECH CO. LTD. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Jan 15, 2034.

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 ROCHE MOLECULAR SYSTEMS, INC, HANGZHOU ALLTEST BIOTECH CO. LTD, 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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81325990322
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Registration Details
ANVISA Registration Number: 81325990322
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Teste Rápido em Cassete para GDH da Clostridium difficile (Fezes)
Risk Class III

Registration Details

81325990322

25351547675202363

19933144000129

Company Information

China
PT: CHINA, REPĂšBLICA POPULAR

Dates and Status

Jan 15, 2024

15/01/2034

09/18/2025 19:00:01

Família Teste Rápido em Cassete para GDH da Clostridium difficile (Fezes)
Risk Class III

Registration Details

81325990322

25351547675202363

19933144000129

Dates and Status

Jan 15, 2024

15/01/2034

09/18/2025 19:00:01