ANVISA registration 81552290016Valid until Apr 15, 2034TREPONEMA PALLIDUM
ANVISA Registration Number: 81552290016SETTY ASSESSORIA E CONSULTORIA EM ASSUNTOS REGULATORIOS LTDAQINGDAO HIGHTOP BIOTECH CO.,LTD.Risk Class IV
Device names
- Commercial name
- FAMÍLIA TESTE RÁPIDO DE ANTICORPO DE SÍFILIS (Treponema Pallidum)
- Risk class
- Class IV
Registration details
- Registration Number
- 81552290016
- Process Number
- 25351336358202313
- 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
- Apr 15, 2024
- Validity
- 15/04/2034
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for TREPONEMA PALLIDUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81552290016 and manufactured by QINGDAO HIGHTOP BIOTECH CO.,LTD.. The registration is held by SETTY ASSESSORIA E CONSULTORIA EM ASSUNTOS REGULATORIOS LTDA with validity until Apr 15, 2034.
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.