Unidirectional Steerable Diagnostic Catheter - FDA Registration 164c4b8ce2f7e72b4432480276792b8f
Access comprehensive regulatory information for Unidirectional Steerable Diagnostic Catheter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 164c4b8ce2f7e72b4432480276792b8f and manufactured by Boston Scientific Corporation. The device was registered on January 05, 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.
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FDA Official Data
164c4b8ce2f7e72b4432480276792b8f
Unidirectional Steerable Diagnostic Catheter
FDA ID: 164c4b8ce2f7e72b4432480276792b8f
Device Classification
Brand Name
Boston Scientific
Registration Information
Analysis ID
164c4b8ce2f7e72b4432480276792b8f
Registration Date
January 05, 2022
Manufacturer
Authorized Representative

