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HumaNex A1c Variant - FDA Registration f83fafe647cab9017eea434963715b6e

Access comprehensive regulatory information for HumaNex A1c Variant in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f83fafe647cab9017eea434963715b6e and manufactured by Gesellschaft fรผr Biochemica und Diagnostica mbH. The device was registered on June 16, 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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f83fafe647cab9017eea434963715b6e
HumaNex A1c Variant
FDA ID: f83fafe647cab9017eea434963715b6e
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Device Classification
Brand Name
Human
Registration Information
Analysis ID
f83fafe647cab9017eea434963715b6e
Registration Date
June 16, 2022