OCCULT BLOOD IN FECES - ANVISA Registration 80638720218

Access comprehensive regulatory information for OCCULT BLOOD IN FECES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80638720218 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Aug 15, 2032.

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 QINGDAO HIGHTOP BIOTECH CO.,LTD., WAMA PRODUTOS PARA LABORATORIO LTDA, 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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80638720218
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Registration Details
ANVISA Registration Number: 80638720218
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FOB RAPID TEST
Risk Class III

Registration Details

80638720218

25351519600202210

11462456000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 15, 2022

15/08/2032

09/18/2025 19:00:01

FOB RAPID TEST
Risk Class III

Registration Details

80638720218

25351519600202210

11462456000190

Company Information

Dates and Status

Aug 15, 2022

15/08/2032

09/18/2025 19:00:01