NeuMoDx™ GBS Test Strip - FDA Registration 69a454f95e62b929967e2e6c1d6d6a8e
Access comprehensive regulatory information for NeuMoDx™ GBS Test Strip in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 69a454f95e62b929967e2e6c1d6d6a8e 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
69a454f95e62b929967e2e6c1d6d6a8e
NeuMoDx™ GBS Test Strip
FDA ID: 69a454f95e62b929967e2e6c1d6d6a8e
Device Classification
Brand Name
QIAGEN
Registration Information
Analysis ID
69a454f95e62b929967e2e6c1d6d6a8e
Registration Date
January 08, 2022
Manufacturer
Authorized Representative

