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QIASTAT-DX® GASTROINTESTINAL PANEL 2, QIASTAT-DX® MENINGITIS/ENCEPHALITIS (ME) PANEL, QIASTAT-DX® RESPIRATORY SARS-COV-2 PANEL. - DIGEMID Registration DMDIV5724E

Access comprehensive regulatory information for QIASTAT-DX® GASTROINTESTINAL PANEL 2, QIASTAT-DX® MENINGITIS/ENCEPHALITIS (ME) PANEL, QIASTAT-DX® RESPIRATORY SARS-COV-2 PANEL. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5724E and manufactured by QIAGEN GmbH. The device was registered on August 28, 2024.

This page provides complete registration details including product type (IN VITRO MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.

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DMDIV5724E
QIASTAT-DX® GASTROINTESTINAL PANEL 2, QIASTAT-DX® MENINGITIS/ENCEPHALITIS (ME) PANEL, QIASTAT-DX® RESPIRATORY SARS-COV-2 PANEL.
DIGEMID ID: DMDIV5724E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5724E
Registration Date
August 28, 2024
Expiration Date
August 28, 2029
Creation Date
March 10, 2025
Manufacturer
Authorized Representative