ANVISA registration 82149920042Valid until Jun 20, 2032CORONAVIRUS
ANVISA Registration Number: 82149920042GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDACERTEST BIOTEC S.L.Risk Class III
Device names
- Commercial name
- VIASURE SARS-CoV-2 Triplex (ORF1ab, E & N genes) Real Time PCR Detection Kit
- Risk class
- Class III
Registration details
- Registration Number
- 82149920042
- Process Number
- 25351281435202391
- CNPJ
- 35489323000175
Company information
- Registration Holder
- GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDA
- Manufacturer
- CERTEST BIOTEC S.L.
- Manufacturing Country
- Spain
PT: ESPANHA
Dates and status
- Publication Date
- Jun 12, 2023
- Validity
- 20/06/2032
- 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 82149920042 and manufactured by CERTEST BIOTEC S.L.. The registration is held by GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDA with validity until Jun 20, 2032.
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