Concentrate Preparation Device - FDA Registration e5bc7c075da764618acd0fb59c898960

Access comprehensive regulatory information for Concentrate Preparation Device in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e5bc7c075da764618acd0fb59c898960 and manufactured by Vivonic GmbH. The device was registered on September 30, 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.