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Fully Automatic PCR - FDA Registration c4e43b8a2dfdf0a296c480eeb5510c91

Access comprehensive regulatory information for Fully Automatic PCR in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c4e43b8a2dfdf0a296c480eeb5510c91 and manufactured by NeuMoDx Molecular, Inc.. The device was registered on October 29, 2021.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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FDA Official Data
c4e43b8a2dfdf0a296c480eeb5510c91
Fully Automatic PCR
FDA ID: c4e43b8a2dfdf0a296c480eeb5510c91
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DJ Fang

DJ Fang

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Device Classification
Brand Name
QIAGEN
Registration Information
Analysis ID
c4e43b8a2dfdf0a296c480eeb5510c91
Registration Date
October 29, 2021
Manufacturer
Authorized Representative