Pure Global

Diagnostic Ultrasound System - FDA Registration 9579fbfe638c5a88a1f02ab444629bda

Access comprehensive regulatory information for Diagnostic Ultrasound System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9579fbfe638c5a88a1f02ab444629bda and manufactured by Shenzhen Mindray Bio Medical Electronics Co., Ltd. The device was registered on October 19, 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.

Free Database
Powered by Pure Global AI
FDA Official Data
9579fbfe638c5a88a1f02ab444629bda
Diagnostic Ultrasound System
FDA ID: 9579fbfe638c5a88a1f02ab444629bda
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Mindray
Registration Information
Analysis ID
9579fbfe638c5a88a1f02ab444629bda
Registration Date
October 19, 2022