ANVISA registration 81313770059ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Commercial name
- FAMÍLIA DE CENTRÍFUGAS LABORATORIAIS SPIN MAX (80-1/80-2)
- Risk class
- Class I
- Registration Number
- 81313770059
- Process Number
- 25351389054202430
- CNPJ
- 07760277000323
- Registration Holder
- MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES LTDA ME
- Manufacturer
- JIANGSU XINKANG MEDICAL INSTRUMENTS CO., LTD
- Manufacturing Country
- China
- Publication Date
- Nov 04, 2024
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
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 81313770059 and manufactured by JIANGSU XINKANG MEDICAL INSTRUMENTS CO., LTD. The registration is held by MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES LTDA ME with validity until currently active (VIGENTE).
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