ANVISA registration 82149920172Valid until Jul 06, 2036COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III
ANVISA Registration Number: 82149920172GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDACERTEST BIOTEC, S.L.Risk Class III
Device names
- Technical name
- COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III
- Commercial name
- VIASURE Herpes virus 1, Herpes virus 2 & Varicella Zoster Virus Real Time PCR Detection Kit Tubes
- Risk class
- Class III
PT: PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Registration details
- Registration Number
- 82149920172
- Process Number
- 25351096255202658
- 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
- Jul 06, 2026
- Validity
- 06/07/2036
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82149920172 and manufactured by CERTEST BIOTEC, S.L.. The registration is held by GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDA with validity until Jul 06, 2036.
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