ANVISA registration 10337990012ActiveInstrumento para preparo e processamento de amostras – fase pré-analítica
ANVISA Registration Number: 10337990012LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA.LEICA BIOSYSTEMS MELBOURNE PTY 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
- 10337990012
- Process Number
- 25351560794201511
- CNPJ
- 52201456000113
Company information
- Registration Holder
- LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA.
- Manufacturer
- LEICA BIOSYSTEMS MELBOURNE PTY LTD
- Manufacturing Country
- Australia
PT: AUSTRÁLIA
Dates and status
- Publication Date
- Nov 03, 2015
- Status
- Active
Official value: VIGENTE
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 10337990012 and manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD. The registration is held by LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA. with validity until currently active (VIGENTE).
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