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POLYSITE - FDA Registration d302f60fe119aa5e5b2e6f9b3911b851

Access comprehensive regulatory information for POLYSITE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d302f60fe119aa5e5b2e6f9b3911b851 and manufactured by PEROUSE MEDICAL. The device was registered on February 23, 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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d302f60fe119aa5e5b2e6f9b3911b851
POLYSITE
FDA ID: d302f60fe119aa5e5b2e6f9b3911b851
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Device Classification
Brand Name
PEROUSE MEDICAL
Registration Information
Analysis ID
d302f60fe119aa5e5b2e6f9b3911b851
Registration Date
February 23, 2022
Manufacturer
Authorized Representative