Myanmar FDA registration cba884000cac1535856cb1513858229a

X-Ray Angiography, Fluoroscopic, Radiographic System

Myanmar·Siemens·Siemens Shenzhen Magnetic Resonance Ltd.·Registered October 15, 2022

Device classification

Brand Name: Siemens

Registration information

Analysis ID: cba884000cac1535856cb1513858229a
Registration Date: October 15, 2022

Manufacturer

Name: Siemens Shenzhen Magnetic Resonance Ltd.

Authorized Representative

Name: MEDITECH COMPANY LIMITED

About this record

Access comprehensive regulatory information for X-Ray Angiography, Fluoroscopic, Radiographic System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cba884000cac1535856cb1513858229a and manufactured by Siemens Shenzhen Magnetic Resonance Ltd.. The device was registered on October 15, 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.