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ANVISA registration 10330660323Valid until Nov 03, 2030

CORONAVIRUS

ANVISA Registration Number: 10330660323DESCARPACK DESCARTAVEIS DO BRASIL LTDASD BIOSENSOR, INC.Risk Class III
Verified
Device names
Technical name
CORONAVIRUS
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PT: CORONAVÍRUS
Commercial name
Teste Rápido Standard Q COVID-19 IgM/IgG COMBO
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Risk class
Class III
Registration details
Registration Number
10330660323
Process Number
25351603875202061
CNPJ
01057428000133
Company information
Registration Holder
DESCARPACK DESCARTAVEIS DO BRASIL LTDA
Manufacturer
SD BIOSENSOR, INC.
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
Nov 03, 2020
Validity
03/11/2030
Last Updated
08/18/2026 19:00:00
About this record

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 10330660323 and manufactured by SD BIOSENSOR, INC.. The registration is held by DESCARPACK DESCARTAVEIS DO BRASIL LTDA with validity until Nov 03, 2030.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.