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Lower Gastrointestinal Endoscope - FDA Registration ec0a41efebd15cd9e6960cb02c91e02f

Access comprehensive regulatory information for Lower Gastrointestinal Endoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ec0a41efebd15cd9e6960cb02c91e02f and manufactured by FUJIFILM Healthcare Manufacturing Coroporation Sano Office. The device was registered on September 22, 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
ec0a41efebd15cd9e6960cb02c91e02f
Lower Gastrointestinal Endoscope
FDA ID: ec0a41efebd15cd9e6960cb02c91e02f
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DJ Fang

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Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
ec0a41efebd15cd9e6960cb02c91e02f
Registration Date
September 22, 2022