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Dialyzer (Polyethersulfone) - FDA Registration 8189c6a03bc094db65a0237a009903df

Access comprehensive regulatory information for Dialyzer (Polyethersulfone) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8189c6a03bc094db65a0237a009903df and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on March 21, 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
8189c6a03bc094db65a0237a009903df
Dialyzer (Polyethersulfone)
FDA ID: 8189c6a03bc094db65a0237a009903df
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Device Classification
Brand Name
HOSPITECH
Registration Information
Analysis ID
8189c6a03bc094db65a0237a009903df
Registration Date
March 21, 2022