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ANVISA registration 10322259003Active

EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS

ANVISA Registration Number: 10322259003QIAGEN BIOTECNOLOGIA BRASIL LTDA.QIAGEN INSTRUMENTSRisk Class I
Verified
Device names
Technical name
EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS
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PT: EQUIPAMENTO PARA PREPARO DE AMOSTRAS PARA DIAGNÓSTICO IN VITRO
Commercial name
BIOROBOT MDX DSP
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Risk class
Class I
Registration details
Registration Number
10322259003
Process Number
25351079297201016
CNPJ
01334250000120
Company information
Registration Holder
QIAGEN BIOTECNOLOGIA BRASIL LTDA.
Manufacturer
QIAGEN INSTRUMENTS
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Jul 30, 2010
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 10322259003 and manufactured by QIAGEN INSTRUMENTS. The registration is held by QIAGEN BIOTECNOLOGIA BRASIL 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.