Myanmar FDA registration 978aa6704a90bd0db41f596c6ec3575a

WHOLE BLOOD DILUTING AND SHEATH REAGENT

Myanmar·Hemax·B&E Bio-technology Co., Ltd·Registered December 05, 2022

Device classification

Brand Name: Hemax

Registration information

Analysis ID: 978aa6704a90bd0db41f596c6ec3575a
Registration Date: December 05, 2022

Manufacturer

Name: B&E Bio-technology Co., Ltd

Authorized Representative

Name: BIZ-PARTNER GROUP COMPANY LIMITED

About this record

Access comprehensive regulatory information for WHOLE BLOOD DILUTING AND SHEATH REAGENT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 978aa6704a90bd0db41f596c6ec3575a and manufactured by B&E Bio-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.