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STREPTOCOCCUS - ANVISA Registration 10071770896

Access comprehensive regulatory information for STREPTOCOCCUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10071770896 and manufactured by ABBOTT DIAGNOSTICS SCARBOROUGH, INC. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until Dec 03, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VEDALAB, Eco Diagnostica 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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10071770896
2 Related Devices
Registration Details
ANVISA Registration Number: 10071770896
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Related Devices (2)

Família ID NOW Strep A 2
Risk Class III

Registration Details

10071770896

25351634406201879

50248780000161

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 03, 2018

03/12/2028

09/18/2025 19:00:01

Família ID NOW Strep A 2
Risk Class III

Registration Details

10071770896

25351634406201879

50248780000161

Company Information

Dates and Status

Dec 03, 2018

03/12/2028

09/18/2025 19:00:01