Myanmar FDA registration 98386aa50e897c7616da8684908e18b8

PES Plus Dialyzer (LOW FLUX)

Myanmar·SATORI·Hospitech Manufacturing Services Sdn. Bhd.·Registered May 02, 2022

Device classification

Brand Name: SATORI

Registration information

Analysis ID: 98386aa50e897c7616da8684908e18b8
Registration Date: May 02, 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 (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.