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Hemodialysis Blood Tubing Set - FDA Registration e321f9fac1ab4e1f2dc4659f7b469fcf

Access comprehensive regulatory information for Hemodialysis Blood Tubing Set in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e321f9fac1ab4e1f2dc4659f7b469fcf and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on March 20, 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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e321f9fac1ab4e1f2dc4659f7b469fcf
Hemodialysis Blood Tubing Set
FDA ID: e321f9fac1ab4e1f2dc4659f7b469fcf
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Device Classification
Brand Name
HOSPITECH
Registration Information
Analysis ID
e321f9fac1ab4e1f2dc4659f7b469fcf
Registration Date
March 20, 2022