ANVISA registration 10337990042ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 10337990042LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA.LEICA BIOSYSTEMS NUSSLOCH GMBHRisk Class I
Device names
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Risk class
- Class I
Registration details
- Registration Number
- 10337990042
- Process Number
- 25351637361201975
- CNPJ
- 52201456000113
Company information
- Registration Holder
- LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA.
- Manufacturer
- LEICA BIOSYSTEMS NUSSLOCH GMBH
- Manufacturing Country
- Germany
PT: ALEMANHA
Dates and status
- Publication Date
- Nov 13, 2019
- 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 10337990042 and manufactured by LEICA BIOSYSTEMS NUSSLOCH GMBH. The registration is held by LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA. with validity until currently active (VIGENTE).
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