ANVISA registration 82832860050ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 82832860050QLX DIAGNÓSTICOS LTDABIOBASE BIODUSTRY (SHANDONG) CO., LTDRisk Class I
Device names
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Risk class
- Class I
Registration details
- Registration Number
- 82832860050
- Process Number
- 25351025617202545
- CNPJ
- 38030634000160
Company information
- Registration Holder
- QLX DIAGNÓSTICOS LTDA
- Manufacturer
- BIOBASE BIODUSTRY (SHANDONG) CO., LTD
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Apr 07, 2025
- 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 82832860050 and manufactured by BIOBASE BIODUSTRY (SHANDONG) CO., LTD. The registration is held by QLX DIAGNÓSTICOS 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.