Myanmar FDA registration be7e6766760492dee3784ab7248fc259

MRI System

Myanmar·Siemens·Siemens Shenzhen Magnetic Resonance Ltd.·Registered June 28, 2022

Device classification

Brand Name: Siemens

Registration information

Analysis ID: be7e6766760492dee3784ab7248fc259
Registration Date: June 28, 2022

Manufacturer

Name: Siemens Shenzhen Magnetic Resonance Ltd.

Authorized Representative

Name: MEDITECH COMPANY LIMITED

About this record

Access comprehensive regulatory information for MRI System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID be7e6766760492dee3784ab7248fc259 and manufactured by Siemens Shenzhen Magnetic Resonance Ltd.. The device was registered on June 28, 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.