Pure Global

Direct Digitizer - FDA Registration d4187a0a7d5f34780cd01a570e69b4a3

Access comprehensive regulatory information for Direct Digitizer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d4187a0a7d5f34780cd01a570e69b4a3 and manufactured by iRay Technology Co.,Ltd.. The device was registered on August 12, 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
d4187a0a7d5f34780cd01a570e69b4a3
Direct Digitizer
FDA ID: d4187a0a7d5f34780cd01a570e69b4a3
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Konica Minolta
Registration Information
Analysis ID
d4187a0a7d5f34780cd01a570e69b4a3
Registration Date
August 12, 2022
Manufacturer
Authorized Representative