Myanmar FDA registration 5128e2592d1f5e0331be9e7562760c07

Influenza A+B Rapid Test Cassette (Swab/Nasal aspirate)

Myanmar·RightSign·Hangzhou Biotest Biotech Co., Ltd.·Registered January 26, 2022

Device classification

Brand Name: RightSign

Registration information

Analysis ID: 5128e2592d1f5e0331be9e7562760c07
Registration Date: January 26, 2022

Manufacturer

Name: Hangzhou Biotest Biotech Co., Ltd.

Authorized Representative

Name: FOCUS HEALTH COMPANY LIMITED

About this record

Access comprehensive regulatory information for Influenza A+B Rapid Test Cassette (Swab/Nasal aspirate) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5128e2592d1f5e0331be9e7562760c07 and manufactured by Hangzhou Biotest Biotech Co., Ltd.. The device was registered on January 26, 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.