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Myanmar FDA registration fdd2cb23d805e996c745a70d022f87ea

Electrolyte Reagent (ISE, Pressure Method), DS-Ⅰ (NO.3)

Myanmar flagMyanmar·GENRUI·Genrui Biotech Inc.·Registered August 16, 2022
Device classification
Brand Name
GENRUI
Registration information
Analysis ID
fdd2cb23d805e996c745a70d022f87ea
Registration Date
August 16, 2022
Manufacturer
Name
Genrui Biotech Inc.
Authorized Representative
Name
GRAND MEDI CORE COMPANY LIMITED
About this record

Access comprehensive regulatory information for Electrolyte Reagent (ISE, Pressure Method), DS-Ⅰ (NO.3) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fdd2cb23d805e996c745a70d022f87ea and manufactured by Genrui Biotech Inc.. The device was registered on August 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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