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Probe-cleaner - FDA Registration d428075af9842976218fb9c35ee7a347

Access comprehensive regulatory information for Probe-cleaner in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d428075af9842976218fb9c35ee7a347 and manufactured by B&E Bio-technology Co., Ltd. The device was registered on December 05, 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
d428075af9842976218fb9c35ee7a347
Probe-cleaner
FDA ID: d428075af9842976218fb9c35ee7a347
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Device Classification
Brand Name
Hemax
Registration Information
Analysis ID
d428075af9842976218fb9c35ee7a347
Registration Date
December 05, 2022
Authorized Representative