Myanmar FDA registration 60d37ec534b67770b74a6d9d5dfb6a44
NeuMoDx™ Cartridge
Device classification
- Brand Name
- QIAGEN
Registration information
- Analysis ID
- 60d37ec534b67770b74a6d9d5dfb6a44
- Registration Date
- January 08, 2022
Manufacturer
Authorized Representative
About this record
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.
Free DatabasePowered by Pure Global AIFDA Official Data