Myanmar FDA registration 4aed038fcbb5e8a4e517a4242caf0f2f

MAGLUMI® Pepsinogen I (CLIA)

Myanmar·Maglumi·Shenzhen New Industries Biomedical Engineering Co., Ltd.·Registered November 15, 2022

Device classification

Brand Name: Maglumi

Registration information

Analysis ID: 4aed038fcbb5e8a4e517a4242caf0f2f
Registration Date: November 15, 2022

Manufacturer

Name: Shenzhen New Industries Biomedical Engineering Co., Ltd.

Authorized Representative

Name: BIOMED MYANMAR COMPANY LIMITED

About this record

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.