Myanmar FDA registration 1b5bf83d0aff25280238f1c82c149388

Refill solution for Reference Electrode

Myanmar·Cornley·Meizhou Cornley Hi-Tech Co., Ltd.·Registered December 21, 2021

Device classification

Brand Name: Cornley

Registration information

Analysis ID: 1b5bf83d0aff25280238f1c82c149388
Registration Date: December 21, 2021

Manufacturer

Name: Meizhou Cornley Hi-Tech Co., Ltd.

Authorized Representative

Name: BIOMED MYANMAR COMPANY LIMITED

About this record

Access comprehensive regulatory information for Refill solution for Reference Electrode in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1b5bf83d0aff25280238f1c82c149388 and manufactured by Meizhou Cornley Hi-Tech Co., Ltd.. The device was registered on December 21, 2021.

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.