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INTERFERON A/B/Y - ANVISA Registration 10322250079

Access comprehensive regulatory information for INTERFERON A/B/Y in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10322250079 and manufactured by QIAGEN. The registration is held by QIAGEN BIOTECNOLOGIA BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including QIAGEN, and 1 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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10322250079
Registration Details
ANVISA Registration Number: 10322250079
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Device Details

QuantiFERON Monitor LyoSphere
Risk Class II

Registration Details

10322250079

25351202367201747

01334250000120

Company Information

QIAGEN
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Oct 31, 2017

VIGENTE

09/18/2025 19:00:01

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