Myanmar FDA registration 65f24e8ad98998c7283993ec272e8c1f

Single Use 3-Lumen Extraction Balloon V

Myanmar·Olympus·Aomori Olympus Co., Ltd·Registered September 12, 2022

Device classification

Brand Name: Olympus

Registration information

Analysis ID: 65f24e8ad98998c7283993ec272e8c1f
Registration Date: September 12, 2022

Manufacturer

Name: Aomori Olympus Co., Ltd

Authorized Representative

Name: YEE SHIN COMPANY LIMITED

About this record

Access comprehensive regulatory information for Single Use 3-Lumen Extraction Balloon V in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 65f24e8ad98998c7283993ec272e8c1f and manufactured by Aomori Olympus Co., Ltd. The device was registered on September 12, 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.