ANVISA registration 10337990021ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 10337990021LEICA 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
- Commercial name
- Família de Instrumentos para diagnósticvo in vitro - Micrótomo Motorizado Leica
- Risk class
- Class I
Registration details
- Registration Number
- 10337990021
- Process Number
- 25351427520201763
- 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
- Oct 02, 2017
- 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 10337990021 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).
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.