Imidazole Buffer Solution - FDA Registration 328deb61ec5c6df23cf2948ac6f32ab4
Access comprehensive regulatory information for Imidazole Buffer Solution in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 328deb61ec5c6df23cf2948ac6f32ab4 and manufactured by Siemens Healthcare Diagnostics products GmbH. The device was registered on December 14, 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
328deb61ec5c6df23cf2948ac6f32ab4
Imidazole Buffer Solution
FDA ID: 328deb61ec5c6df23cf2948ac6f32ab4
Device Classification
Brand Name
Siemens
Registration Information
Analysis ID
328deb61ec5c6df23cf2948ac6f32ab4
Registration Date
December 14, 2022
Manufacturer
Authorized Representative

