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Vitamin B12 (eCLIA) - FDA Registration 1576c30de7cd33f1eefb7779114cb082

Access comprehensive regulatory information for Vitamin B12 (eCLIA) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1576c30de7cd33f1eefb7779114cb082 and manufactured by Shenzhen Lifotronic Technology Co.,ltd. The device was registered on March 27, 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
1576c30de7cd33f1eefb7779114cb082
Vitamin B12 (eCLIA)
FDA ID: 1576c30de7cd33f1eefb7779114cb082
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Device Classification
Brand Name
Lifotronic
Registration Information
Analysis ID
1576c30de7cd33f1eefb7779114cb082
Registration Date
March 27, 2022
Authorized Representative