Thyroid Stimulating Hormone ( TSH ) Diagnostic Kit - FDA Registration 513d32c7be39d0c89f01d08e389d312a
Access comprehensive regulatory information for Thyroid Stimulating Hormone ( TSH ) Diagnostic Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 513d32c7be39d0c89f01d08e389d312a and manufactured by Shenzhen Microprofit Biotech Co.,Ltd.. The device was registered on February 02, 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
513d32c7be39d0c89f01d08e389d312a
Thyroid Stimulating Hormone ( TSH ) Diagnostic Kit
FDA ID: 513d32c7be39d0c89f01d08e389d312a
Local name: Thyroid Stimulating Hormone ๏ผ TSH ๏ผ Diagnostic Kit
Device Classification
Brand Name
Fluorecare
Registration Information
Analysis ID
513d32c7be39d0c89f01d08e389d312a
Registration Date
February 02, 2022
Manufacturer
Authorized Representative

