PES Plus Dialyzer (HIGH FLUX) - FDA Registration c53fd196b69c1dff8703a39cd20729f5
Access comprehensive regulatory information for PES Plus Dialyzer (HIGH FLUX) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c53fd196b69c1dff8703a39cd20729f5 and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on April 26, 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
c53fd196b69c1dff8703a39cd20729f5
PES Plus Dialyzer (HIGH FLUX)
FDA ID: c53fd196b69c1dff8703a39cd20729f5
Device Classification
Brand Name
SATORI
Registration Information
Analysis ID
c53fd196b69c1dff8703a39cd20729f5
Registration Date
April 26, 2022
Manufacturer
Authorized Representative

