HEMODIALYSIS BLOOD TUBING SET - FDA Registration 7895a434a0aac82c742e6d4b2f4bd916
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 7895a434a0aac82c742e6d4b2f4bd916 and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on July 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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FDA Official Data
7895a434a0aac82c742e6d4b2f4bd916
HEMODIALYSIS BLOOD TUBING SET
FDA ID: 7895a434a0aac82c742e6d4b2f4bd916
Device Classification
Brand Name
SATORI
Registration Information
Analysis ID
7895a434a0aac82c742e6d4b2f4bd916
Registration Date
July 20, 2022
Manufacturer
Authorized Representative

