Myanmar FDA registration dc402018ec39cea273d26ea0def492be

ichroma AMH

Myanmar·ichroma·Boditech Med Inc.·Registered November 30, 2022

Device classification

Brand Name: ichroma

Registration information

Analysis ID: dc402018ec39cea273d26ea0def492be
Registration Date: November 30, 2022

Manufacturer

Name: Boditech Med Inc.

Authorized Representative

Name: HEALTHCARE MANDALAR PHARMACEUTICALS AND LABORATORY COMPANY LIMITED

About this record

Access comprehensive regulatory information for ichroma AMH in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dc402018ec39cea273d26ea0def492be 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.