ANVISA registration 80102512363ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 80102512363VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDADRUCKER DIAGNOSTICSRisk Class I
Device names
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Risk class
- Class I
Registration details
- Registration Number
- 80102512363
- Process Number
- 25351670263201940
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- DRUCKER DIAGNOSTICS
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Nov 28, 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 80102512363 and manufactured by DRUCKER DIAGNOSTICS. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).
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