Myanmar FDA registration 1cdb6eebd9ae5cc1b12bc35e5de4e8a5

Evis Exera III Duodenovideoscope & Accessories

Myanmar·Olympus·Aizu Olympus Co., Ltd·Registered November 15, 2021

Device classification

Brand Name: Olympus

Registration information

Analysis ID: 1cdb6eebd9ae5cc1b12bc35e5de4e8a5
Registration Date: November 15, 2021

Manufacturer

Name: Aizu Olympus Co., Ltd

Authorized Representative

Name: YEE SHIN COMPANY LIMITED

About this record

Access comprehensive regulatory information for Evis Exera III Duodenovideoscope & Accessories in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1cdb6eebd9ae5cc1b12bc35e5de4e8a5 and manufactured by Aizu Olympus Co., Ltd. The device was registered on November 15, 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.