Myanmar FDA registration 51858d6ed504a13c44498471ba583dda

Scalp Vein Set for single use

Myanmar·Haodi·Yunnan Haodi Medical Instrument Co.,Ltd·Registered July 01, 2022

Device classification

Brand Name: Haodi

Registration information

Analysis ID: 51858d6ed504a13c44498471ba583dda
Registration Date: July 01, 2022

Manufacturer

Name: Yunnan Haodi Medical Instrument Co.,Ltd

Authorized Representative

Name: PAI BROTHERS INTERNATIONAL TRADING COMPANY LIMITED

About this record

Access comprehensive regulatory information for Scalp Vein Set for single use in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 51858d6ed504a13c44498471ba583dda and manufactured by Yunnan Haodi Medical Instrument Co.,Ltd. The device was registered on July 01, 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.