Pure Global

Contract Media Injector (CT Double Syringe Injection System) - FDA Registration 5a30e498873951965e69b4e1e00b72b0

Access comprehensive regulatory information for Contract Media Injector (CT Double Syringe Injection System) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5a30e498873951965e69b4e1e00b72b0 and manufactured by Shenzhen Seacrown Electromechanical Co.Ltd. The device was registered on March 26, 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
5a30e498873951965e69b4e1e00b72b0
Contract Media Injector (CT Double Syringe Injection System)
FDA ID: 5a30e498873951965e69b4e1e00b72b0
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Seacrown
Registration Information
Analysis ID
5a30e498873951965e69b4e1e00b72b0
Registration Date
March 26, 2022
Authorized Representative