Myanmar FDA registration 7895a434a0aac82c742e6d4b2f4bd916

HEMODIALYSIS BLOOD TUBING SET

Myanmar·SATORI·Hospitech Manufacturing Services Sdn. Bhd.·Registered July 20, 2022

Device classification

Brand Name: SATORI

Registration information

Analysis ID: 7895a434a0aac82c742e6d4b2f4bd916
Registration Date: July 20, 2022

Manufacturer

Name: Hospitech Manufacturing Services Sdn. Bhd.

Authorized Representative

Name: HEALTHCARE MANDALAR PHARMACEUTICALS AND LABORATORY COMPANY LIMITED

About this record

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.