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Phosphorus Kit (Mod. Gomorri's Method) - FDA Registration 4d5e4511907320038974011a156eaab1

Access comprehensive regulatory information for Phosphorus Kit (Mod. Gomorri's Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4d5e4511907320038974011a156eaab1 and manufactured by Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.. The device was registered on June 15, 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.

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4d5e4511907320038974011a156eaab1
Phosphorus Kit (Mod. Gomorri's Method)
FDA ID: 4d5e4511907320038974011a156eaab1
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Device Classification
Brand Name
Coral Clinical Systems
Registration Information
Analysis ID
4d5e4511907320038974011a156eaab1
Registration Date
June 15, 2022