Myanmar FDA registration 003a8fb524b4773dab78c03454fcca1a

MaxLINE HBsAg Rapid Test Device Serum/Plasma

Myanmar·MaxLINE·Avecon Healthcare Pvt. Ltd.·Registered July 27, 2022

Device classification

Brand Name: MaxLINE

Registration information

Analysis ID: 003a8fb524b4773dab78c03454fcca1a
Registration Date: July 27, 2022

Manufacturer

Name: Avecon Healthcare Pvt. Ltd.

Authorized Representative

Name: DEW MEDICAL AND DIAGNOSTIC (DMD) COMPANY LIMITED

About this record

Access comprehensive regulatory information for MaxLINE HBsAg Rapid Test Device Serum/Plasma in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 003a8fb524b4773dab78c03454fcca1a and manufactured by Avecon Healthcare Pvt. Ltd.. The device was registered on July 27, 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.