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MAGLUMI® Pepsinogen I (CLIA) - FDA Registration 4aed038fcbb5e8a4e517a4242caf0f2f

Access comprehensive regulatory information for MAGLUMI® Pepsinogen I (CLIA) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4aed038fcbb5e8a4e517a4242caf0f2f 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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4aed038fcbb5e8a4e517a4242caf0f2f
MAGLUMI® Pepsinogen I (CLIA)
FDA ID: 4aed038fcbb5e8a4e517a4242caf0f2f
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Device Classification
Brand Name
Maglumi
Registration Information
Analysis ID
4aed038fcbb5e8a4e517a4242caf0f2f
Registration Date
November 15, 2022