Myanmar FDA registration e321f9fac1ab4e1f2dc4659f7b469fcf
Hemodialysis Blood Tubing Set
Device classification
- Brand Name
- HOSPITECH
Registration information
- Analysis ID
- e321f9fac1ab4e1f2dc4659f7b469fcf
- Registration Date
- March 20, 2022
Manufacturer
Authorized Representative
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 e321f9fac1ab4e1f2dc4659f7b469fcf and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on March 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.
Free DatabasePowered by Pure Global AIFDA Official Data