Myanmar FDA registration 6e521c620197e61ae26edf0cedbac0c2

Angiography System

Myanmar·Siemens·Siemens Healthcare GmbH·Registered November 18, 2022

Device classification

Brand Name: Siemens

Registration information

Analysis ID: 6e521c620197e61ae26edf0cedbac0c2
Registration Date: November 18, 2022

Manufacturer

Name: Siemens Healthcare GmbH

Authorized Representative

Name: MEDITECH COMPANY LIMITED

About this record

Access comprehensive regulatory information for Angiography System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6e521c620197e61ae26edf0cedbac0c2 and manufactured by Siemens Healthcare GmbH. The device was registered on November 18, 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.