CK-MB Rapid Quantitative Test - FDA Registration 4622eb4511711220edaeabcc10662370

Access comprehensive regulatory information for CK-MB Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4622eb4511711220edaeabcc10662370 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on September 09, 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.