Myanmar FDA registration 70a0affb63533223db112be7a0ab66e8

Flexilus II Laparoscope

Myanmar·COVIDIEN·Scholly Fiberoptic GmbH·Registered December 08, 2022

Device classification

Brand Name: COVIDIEN

Registration information

Analysis ID: 70a0affb63533223db112be7a0ab66e8
Registration Date: December 08, 2022

Manufacturer

Name: Scholly Fiberoptic GmbH

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

Access comprehensive regulatory information for Flexilus II Laparoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 70a0affb63533223db112be7a0ab66e8 and manufactured by Scholly Fiberoptic GmbH. The device was registered on December 08, 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.