Pure Global AI
ANVISA registration 80153030151Active

Instrumento para preparo e processamento de amostras – fase pré-analítica

ANVISA Registration Number: 80153030151MONTSERRAT COMERCIAL IMPORTADORA E EXPORTADORA LTDAZENITH LAB (JIANGSU) CO., LTD.Risk Class I
Device names
Technical name
Instrumento para preparo e processamento de amostras – fase pré-analítica
Commercial name
FAMÍLIA DE CENTRÍFUGAS MONTSERRAT
Risk class
Class I
Registration details
Registration Number
80153030151
Process Number
25351107154201818
CNPJ
66581935000117
Company information
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 04, 2018
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrumento para preparo e processamento de amostras – fase pré-analítica in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80153030151 and manufactured by ZENITH LAB (JIANGSU) CO., LTD.. The registration is held by MONTSERRAT COMERCIAL IMPORTADORA E EXPORTADORA 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.