ANVISA registration 10338930281ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 10338930281EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDAHANGZHOU ALLSHENG INSTRUMENTS CO., LTD.Risk Class I
Device names
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Risk class
- Class I
Registration details
- Registration Number
- 10338930281
- Process Number
- 25351492047202252
- CNPJ
- 93741726000166
Company information
- Registration Holder
- EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
- Manufacturer
- HANGZHOU ALLSHENG INSTRUMENTS CO., LTD.
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- May 12, 2022
- 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 10338930281 and manufactured by HANGZHOU ALLSHENG INSTRUMENTS CO., LTD.. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until currently active (VIGENTE).
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