NeuMoDx™ Vantage Viral Lysis Buffer - FDA Registration f1a4b54e69daf1cdb510bbcc706c14c8
Access comprehensive regulatory information for NeuMoDx™ Vantage Viral Lysis Buffer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f1a4b54e69daf1cdb510bbcc706c14c8 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
f1a4b54e69daf1cdb510bbcc706c14c8
NeuMoDx™ Vantage Viral Lysis Buffer
FDA ID: f1a4b54e69daf1cdb510bbcc706c14c8
Device Classification
Brand Name
NeuMoDx™
Registration Information
Analysis ID
f1a4b54e69daf1cdb510bbcc706c14c8
Registration Date
January 08, 2022
Manufacturer
Authorized Representative

