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URETERAL Balloon Dilator - FDA Registration a1edd07210f207a9d7b109c7f42739d3

Access comprehensive regulatory information for URETERAL Balloon Dilator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a1edd07210f207a9d7b109c7f42739d3 and manufactured by Blue Neem Medical Devices Private Limited. The device was registered on February 01, 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
a1edd07210f207a9d7b109c7f42739d3
URETERAL Balloon Dilator
FDA ID: a1edd07210f207a9d7b109c7f42739d3
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Device Classification
Brand Name
BLUENEEM
Registration Information
Analysis ID
a1edd07210f207a9d7b109c7f42739d3
Registration Date
February 01, 2022