EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS
ANVISA Registration Number: 10337990011LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA.Leica Biosystems Nussloch GmbHRisk Class I
Device names
- Technical name
- EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS
- Risk class
- Class I
PT: EQUIPAMENTO PARA PREPARO DE AMOSTRAS PARA DIAGNÓSTICO IN VITRO
Registration details
- Registration Number
- 10337990011
- Process Number
- 25351560681201513
- 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 03, 2015
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10337990011 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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