GLYCOSYLATED HEMOGLOBIN KIT - FDA Registration 3cf18709eb7a1be15381b1e24f854360
Access comprehensive regulatory information for GLYCOSYLATED HEMOGLOBIN KIT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3cf18709eb7a1be15381b1e24f854360 and manufactured by Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.. The device was registered on May 20, 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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FDA Official Data
3cf18709eb7a1be15381b1e24f854360
GLYCOSYLATED HEMOGLOBIN KIT
FDA ID: 3cf18709eb7a1be15381b1e24f854360
Device Classification
Brand Name
Coral Clinical Systems
Registration Information
Analysis ID
3cf18709eb7a1be15381b1e24f854360
Registration Date
May 20, 2022
Authorized Representative

