Self-test instrument for glucose - ANVISA Registration 10160610100

Access comprehensive regulatory information for Self-test instrument for glucose in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10160610100 and manufactured by manufacturer not specified. The registration is held by INJEX INDÚSTRIAS CIRÚRGICAS LTDA with validity until Feb 11, 2029.

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 OK BIOTECH CO., LTD., TIANJIN EMPECS MEDICAL DEVICE 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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10160610100
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Registration Details
ANVISA Registration Number: 10160610100
Janaina dos Santos de Miranda

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Related Devices (2)

MEDIDOR DE GLICOSE INJEX SENS PRO
Risk Class III

Registration Details

10160610100

25351609812201801

59309302000199

Company Information

Dates and Status

Feb 11, 2019

11/02/2029

09/18/2025 19:00:01

MEDIDOR DE GLICOSE INJEX SENS PRO
Risk Class III

Registration Details

10160610100

25351609812201801

59309302000199

Company Information

I-SENS, INC
South Korea
PT: CORÉIA DO SUL

Dates and Status

Feb 11, 2019

11/02/2029

09/18/2025 19:00:01