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Compressor Nebulizer - FDA Registration 30146615838d80aadff536a1c962d490

Access comprehensive regulatory information for Compressor Nebulizer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 30146615838d80aadff536a1c962d490 and manufactured by Rossmax Swiss GmbH, Switzerland. The device was registered on August 19, 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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30146615838d80aadff536a1c962d490
Compressor Nebulizer
FDA ID: 30146615838d80aadff536a1c962d490
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Device Classification
Brand Name
Accumed
Registration Information
Analysis ID
30146615838d80aadff536a1c962d490
Registration Date
August 19, 2022