Single Use Aspiration Needle (EZ Shot3) - FDA Registration 2d00f4706011c2bb37bfd33e8ca2ab30
Access comprehensive regulatory information for Single Use Aspiration Needle (EZ Shot3) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2d00f4706011c2bb37bfd33e8ca2ab30 and manufactured by Aomori Olympus Co., Ltd. The device was registered on September 07, 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
2d00f4706011c2bb37bfd33e8ca2ab30
Single Use Aspiration Needle (EZ Shot3)
FDA ID: 2d00f4706011c2bb37bfd33e8ca2ab30
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
2d00f4706011c2bb37bfd33e8ca2ab30
Registration Date
September 07, 2022
Manufacturer
Authorized Representative

