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NeuMoDx™ SARS-CoV-2 Test Strip - FDA Registration a2a0e480006b59e4cf1eb39f75360050

Access comprehensive regulatory information for NeuMoDx™ SARS-CoV-2 Test Strip in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a2a0e480006b59e4cf1eb39f75360050 and manufactured by NeuMoDx Molecular, Inc.. The device was registered on March 28, 2022.

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
a2a0e480006b59e4cf1eb39f75360050
NeuMoDx™ SARS-CoV-2 Test Strip
FDA ID: a2a0e480006b59e4cf1eb39f75360050
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Device Classification
Brand Name
NeuMoDx™
Registration Information
Analysis ID
a2a0e480006b59e4cf1eb39f75360050
Registration Date
March 28, 2022
Manufacturer
Authorized Representative