Myanmar FDA registration c53fd196b69c1dff8703a39cd20729f5

PES Plus Dialyzer (HIGH FLUX)

Myanmar·SATORI·Hospitech Manufacturing Services Sdn. Bhd.·Registered April 26, 2022

Device classification

Brand Name: SATORI

Registration information

Analysis ID: c53fd196b69c1dff8703a39cd20729f5
Registration Date: April 26, 2022

Manufacturer

Name: Hospitech Manufacturing Services Sdn. Bhd.

Authorized Representative

Name: HEALTHCARE MANDALAR PHARMACEUTICAL AND LABORATORY COMPANY LIMITED

About this record

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.