Pure Global

Automated External Defibrillator - FDA Registration 650b4bf8a5ccb979c6d353c5e2969e77

Access comprehensive regulatory information for Automated External Defibrillator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 650b4bf8a5ccb979c6d353c5e2969e77 and manufactured by Shenzhen Mindray Bio- Medical Electronics Co.Ltd. The device was registered on March 25, 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
650b4bf8a5ccb979c6d353c5e2969e77
Automated External Defibrillator
FDA ID: 650b4bf8a5ccb979c6d353c5e2969e77
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
650b4bf8a5ccb979c6d353c5e2969e77
Registration Date
March 25, 2022