SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG) - ANVISA Registration 80954880141

Access comprehensive regulatory information for SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80954880141 and manufactured by Eco Diagnostica Ltda. The registration is held by Eco Diagnostica Ltda with validity until currently active (VIGENTE).

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 HANGZHOU ALLTEST BIOTECH CO. LTD, ALAMAR TECNO CIENTÍFICA 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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80954880141
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Registration Details
ANVISA Registration Number: 80954880141
Janaina dos Santos de Miranda

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Related Devices (2)

Registration Details

80954880141

25351060269202048

14633154000206

Company Information

Brazil
PT: BRASIL

Dates and Status

Jul 20, 2020

VIGENTE

09/18/2025 19:00:01

Registration Details

80954880141

25351060269202048

14633154000206

Company Information

Brazil
PT: BRASIL

Dates and Status

Jul 20, 2020

VIGENTE

09/18/2025 19:00:01