Myanmar FDA registration fdd2cb23d805e996c745a70d022f87ea

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

Name: Electrolyte Reagent (ISE, Pressure Method), DS-Ⅰ (NO.3) — Myanmar FDA registration fdd2cb23d805e996c745a70d022f87ea
Creator: Genrui Biotech Inc.
Keywords: Electrolyte Reagent (ISE, Pressure Method), DS-Ⅰ (NO.3), Electrolyte Reagent (ISE, Pressure Method), DS-Ⅰ (NO.3), GENRUI, fdd2cb23d805e996c745a70d022f87ea, Myanmar FDA registration

MyanmarGENRUIGenrui Biotech Inc.Registered August 16, 2022

VerifiedFDA Myanmar · official registry

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.