PES Plus Dialyzer (LOW FLUX) - FDA Registration 98386aa50e897c7616da8684908e18b8
Access comprehensive regulatory information for PES Plus Dialyzer (LOW FLUX) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 98386aa50e897c7616da8684908e18b8 and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on May 02, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
98386aa50e897c7616da8684908e18b8
PES Plus Dialyzer (LOW FLUX)
FDA ID: 98386aa50e897c7616da8684908e18b8
Device Classification
Brand Name
SATORI
Registration Information
Analysis ID
98386aa50e897c7616da8684908e18b8
Registration Date
May 02, 2022
Manufacturer
Authorized Representative

