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ANVISA registration 81597710022Valid until Aug 03, 2036

HUMAN PAPILLOMAVIRUS (HPV)

ANVISA Registration Number: 81597710022SEEGENE DO BRASIL COMERCIO DE PRODUTOS MEDICOS E HOSPITALARES LTDA.SEEGENE INC.Risk Class III
Verified
Device names
Technical name
HUMAN PAPILLOMAVIRUS (HPV)
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PT: PAPILOMAVÍRUS HUMANO (HPV)
Commercial name
Allplex HPV28 Detection
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Risk class
Class III
Registration details
Registration Number
81597710022
Process Number
25351100094202612
CNPJ
27870531000191
Company information
Registration Holder
SEEGENE DO BRASIL COMERCIO DE PRODUTOS MEDICOS E HOSPITALARES LTDA.
Manufacturer
SEEGENE INC.
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
Aug 03, 2026
Validity
03/08/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for HUMAN PAPILLOMAVIRUS (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 81597710022 and manufactured by SEEGENE INC.. The registration is held by SEEGENE DO BRASIL COMERCIO DE PRODUTOS MEDICOS E HOSPITALARES LTDA. with validity until Aug 03, 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.