ANVISA registration 80638720223Valid until Sep 05, 2032

TREPONEMA PALLIDUM

Name: TREPONEMA PALLIDUM — ANVISA registration 80638720223
Creator: HANGZHOU ALLTEST BIOTECH CO., LTD
Keywords: TREPONEMA PALLIDUM, TREPONEMA PALLIDUM, SÍFILIS RAPID TEST, 80638720223, Risk Class IV, ANVISA registration

ANVISA Registration Number: 80638720223DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - MEHANGZHOU ALLTEST BIOTECH CO., LTDRisk Class IV

Verified

Device names

Technical name: TREPONEMA PALLIDUM
Commercial name: SÍFILIS RAPID TEST
Risk class: Class IV

Registration details

Registration Number: 80638720223
Process Number: 25351516995202291
CNPJ: 11462456000190

Company information

Registration Holder: DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME
Manufacturer: HANGZHOU ALLTEST BIOTECH CO., LTD
Manufacturing Country: China

Dates and status

Publication Date: Sep 05, 2022
Validity: 05/09/2032
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 80638720223 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Sep 05, 2032.

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.