Myanmar FDA registration 56106681ab297152d7ef44582ee41caf

Dengue Ag and Ab Combo Rapid Test Cassette (Whole Blood/ Serum/ Plasma)

Myanmar·RightSign·Hangzhou Biotest Biotech Co., Ltd.·Registered July 01, 2022

Device classification

Brand Name: RightSign

Registration information

Analysis ID: 56106681ab297152d7ef44582ee41caf
Registration Date: July 01, 2022

Manufacturer

Name: Hangzhou Biotest Biotech Co., Ltd.

Authorized Representative

Name: FOCUS HEALTH COMPANY LIMITED

About this record

Access comprehensive regulatory information for Dengue Ag and Ab Combo Rapid Test Cassette (Whole Blood/ Serum/ Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 56106681ab297152d7ef44582ee41caf and manufactured by Hangzhou Biotest Biotech Co., Ltd.. The device was registered on July 01, 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.