Pure Global

ichroma H. pylori SA - FDA Registration b64061b0dd9901e22f700360bab9a31c

Access comprehensive regulatory information for ichroma H. pylori SA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b64061b0dd9901e22f700360bab9a31c and manufactured by Boditech Med Inc.. The device was registered on November 30, 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.

Free Database
Powered by Pure Global AI
FDA Official Data
b64061b0dd9901e22f700360bab9a31c
ichroma H. pylori SA
FDA ID: b64061b0dd9901e22f700360bab9a31c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
ichroma
Registration Information
Analysis ID
b64061b0dd9901e22f700360bab9a31c
Registration Date
November 30, 2022