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CORONAVIRUS - ANVISA Registration 80954880178

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80954880178 and manufactured by SD BIOSENSOR, INC.. The registration is held by Eco Diagnostica Ltda with validity until Oct 04, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO., LTD., 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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80954880178
2 Related Devices
Registration Details
ANVISA Registration Number: 80954880178
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Related Devices (2)

STANDARD Q COVID Ag Saliva
Risk Class III

Registration Details

80954880178

25351301169202168

14633154000206

Company Information

SD BIOSENSOR, INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Oct 04, 2021

04/10/2031

09/18/2025 19:00:01

STANDARD Q COVID Ag Saliva
Risk Class III

Registration Details

80954880178

25351301169202168

14633154000206

Company Information

Dates and Status

Oct 04, 2021

04/10/2031

09/18/2025 19:00:01