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Adenosine deaminase Test Kit (Enzyme Rate Method) - FDA Registration c6bc06d098f993d64d1c216cc0b6f021

Access comprehensive regulatory information for Adenosine deaminase Test Kit (Enzyme Rate Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c6bc06d098f993d64d1c216cc0b6f021 and manufactured by Shijiazhuang Hipro Biotechnology Co.,ltd. The device was registered on October 20, 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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c6bc06d098f993d64d1c216cc0b6f021
Adenosine deaminase Test Kit (Enzyme Rate Method)
FDA ID: c6bc06d098f993d64d1c216cc0b6f021
Local name: Adenosine deaminase Test Kit ๏ผˆEnzyme Rate Method๏ผ‰
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Device Classification
Brand Name
Hiproโ„ข
Registration Information
Analysis ID
c6bc06d098f993d64d1c216cc0b6f021
Registration Date
October 20, 2022