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AIRFLOW PLUS PROPHYLAXIS POWDER - FDA Registration 23b13aed390934b5c612489fe1a8c2d1

Access comprehensive regulatory information for AIRFLOW PLUS PROPHYLAXIS POWDER in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 23b13aed390934b5c612489fe1a8c2d1 and manufactured by EMS Electro Medical System S.A. The device was registered on May 23, 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
23b13aed390934b5c612489fe1a8c2d1
AIRFLOW PLUS PROPHYLAXIS POWDER
FDA ID: 23b13aed390934b5c612489fe1a8c2d1
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Device Classification
Brand Name
EMS Electro Medical System S.A
Registration Information
Analysis ID
23b13aed390934b5c612489fe1a8c2d1
Registration Date
May 23, 2022
Authorized Representative