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Myanmar FDA registration 6e521c620197e61ae26edf0cedbac0c2

Angiography System

MyanmarSiemensSiemens Healthcare GmbHRegistered November 18, 2022
VerifiedFDA Myanmar · official registry
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.