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ANVISA registration 80102513715Valid until Aug 17, 2036

PAPILOMAVÍRUS HUMANO (HPV)

ANVISA Registration Number: 80102513715VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAOSANG HEALTHCARE CO., LTD.Risk Class III
Verified
Device names
Technical name
PAPILOMAVÍRUS HUMANO (HPV)
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Commercial name
GeneFinder HPV-HR RealAmp kit
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Risk class
Class III
Registration details
Registration Number
80102513715
Process Number
25351060040202607
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
OSANG HEALTHCARE CO., LTD.
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
Aug 17, 2026
Validity
17/08/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for PAPILOMAVÍRUS HUMANO (HPV) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513715 and manufactured by OSANG HEALTHCARE CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Aug 17, 2036.

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.