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Endoscopy - FDA Registration e3df16e2bb1c5b4439bd7f41b7d331f0

Access comprehensive regulatory information for Endoscopy in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e3df16e2bb1c5b4439bd7f41b7d331f0 and manufactured by Aizu Olympus Co., Ltd. The device was registered on May 25, 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
e3df16e2bb1c5b4439bd7f41b7d331f0
Endoscopy
FDA ID: e3df16e2bb1c5b4439bd7f41b7d331f0
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Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
e3df16e2bb1c5b4439bd7f41b7d331f0
Registration Date
May 25, 2022
Manufacturer
Authorized Representative