Single Use 3-Lumen Extraction Balloon V - FDA Registration 65f24e8ad98998c7283993ec272e8c1f
Access comprehensive regulatory information for Single Use 3-Lumen Extraction Balloon V in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 65f24e8ad98998c7283993ec272e8c1f and manufactured by Aomori Olympus Co., Ltd. The device was registered on September 12, 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
65f24e8ad98998c7283993ec272e8c1f
Single Use 3-Lumen Extraction Balloon V
FDA ID: 65f24e8ad98998c7283993ec272e8c1f
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
65f24e8ad98998c7283993ec272e8c1f
Registration Date
September 12, 2022
Manufacturer
Authorized Representative

