NeuMoDx™ HCV Test - FDA Registration 4435ec688f0a8c2d4d777fd6792c4a41
Access comprehensive regulatory information for NeuMoDx™ HCV Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4435ec688f0a8c2d4d777fd6792c4a41 and manufactured by NeuMoDx Molecular, Inc.. The device was registered on June 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
4435ec688f0a8c2d4d777fd6792c4a41
NeuMoDx™ HCV Test
FDA ID: 4435ec688f0a8c2d4d777fd6792c4a41
Device Classification
Brand Name
NeuMoDx™
Registration Information
Analysis ID
4435ec688f0a8c2d4d777fd6792c4a41
Registration Date
June 28, 2022
Manufacturer
Authorized Representative

