MAGLUMI® Pepsinogen II (CLIA) - FDA Registration d010c5ff1671f7ed5934b65b4b15843a
Access comprehensive regulatory information for MAGLUMI® Pepsinogen II (CLIA) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d010c5ff1671f7ed5934b65b4b15843a and manufactured by Shenzhen New Industries Biomedical Engineering Co., Ltd.. The device was registered on November 15, 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
d010c5ff1671f7ed5934b65b4b15843a
MAGLUMI® Pepsinogen II (CLIA)
FDA ID: d010c5ff1671f7ed5934b65b4b15843a
Device Classification
Brand Name
Maglumi
Registration Information
Analysis ID
d010c5ff1671f7ed5934b65b4b15843a
Registration Date
November 15, 2022
Manufacturer
Authorized Representative

