Pure Global AI
ANVISA registration 81552290012Active

FERTILITY SELF-TEST

ANVISA Registration Number: 81552290012SETTY ASSESSORIA E CONSULTORIA EM ASSUNTOS REGULATORIOS LTDAQINGDAO HIGHTOP BIOTECH CO.,LTD.Risk Class II
Verified
Device names
Technical name
FERTILITY SELF-TEST
View exact technical-name matches →
PT: AUTOTESTE PARA FERTILIDADE
Commercial name
Teste Rápido de Ovulação LH
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
81552290012
Process Number
25351718399202324
CNPJ
26406496000191
Company information
Registration Holder
SETTY ASSESSORIA E CONSULTORIA EM ASSUNTOS REGULATORIOS LTDA
Manufacturer
QINGDAO HIGHTOP BIOTECH CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 27, 2023
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for FERTILITY SELF-TEST in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81552290012 and manufactured by QINGDAO HIGHTOP BIOTECH CO.,LTD.. The registration is held by SETTY ASSESSORIA E CONSULTORIA EM ASSUNTOS REGULATORIOS LTDA with validity until currently active (VIGENTE).

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.