EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE - FDA Registration d86193245de92b3ffa228411a69c3a50
Access comprehensive regulatory information for EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d86193245de92b3ffa228411a69c3a50 and manufactured by Shirakawa Olympus Co.,Ltd. The device was registered on December 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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d86193245de92b3ffa228411a69c3a50
EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE
FDA ID: d86193245de92b3ffa228411a69c3a50
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
d86193245de92b3ffa228411a69c3a50
Registration Date
December 12, 2022
Manufacturer
Authorized Representative

