NeuMoDx™ Cartridge - FDA Registration 60d37ec534b67770b74a6d9d5dfb6a44
Access comprehensive regulatory information for NeuMoDx™ Cartridge in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 60d37ec534b67770b74a6d9d5dfb6a44 and manufactured by NeuMoDx Molecular, Inc.. The device was registered on January 08, 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
60d37ec534b67770b74a6d9d5dfb6a44
NeuMoDx™ Cartridge
FDA ID: 60d37ec534b67770b74a6d9d5dfb6a44
Device Classification
Brand Name
QIAGEN
Registration Information
Analysis ID
60d37ec534b67770b74a6d9d5dfb6a44
Registration Date
January 08, 2022
Manufacturer
Authorized Representative

