Myanmar FDA registration 6f56afe637373a77ca40aad4084150a2

Reagents for Hemoglobin Analyzer (HPLC) (H8)

Myanmar·Lifotronic·Shenzhen Lifotronic Technology Co., Ltd.·Registered December 05, 2022

Device classification

Brand Name: Lifotronic

Registration information

Analysis ID: 6f56afe637373a77ca40aad4084150a2
Registration Date: December 05, 2022

Manufacturer

Name: Shenzhen Lifotronic Technology Co., Ltd.

Authorized Representative

Name: ZEYA & ASSOCIATES COMPANY LIMITED

About this record

Access comprehensive regulatory information for Reagents for Hemoglobin Analyzer (HPLC) (H8) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6f56afe637373a77ca40aad4084150a2 and manufactured by Shenzhen Lifotronic Technology Co., Ltd.. The device was registered on December 05, 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.