ISE Urine Diluent - FDA Registration 3ccc16a6c346f4d45ebccac9a8d9c4c6
Access comprehensive regulatory information for ISE Urine Diluent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3ccc16a6c346f4d45ebccac9a8d9c4c6 and manufactured by DiaSys Diagnostic Systems GmbH. The device was registered on November 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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FDA Official Data
3ccc16a6c346f4d45ebccac9a8d9c4c6
ISE Urine Diluent
FDA ID: 3ccc16a6c346f4d45ebccac9a8d9c4c6
Device Classification
Brand Name
Diasys
Registration Information
Analysis ID
3ccc16a6c346f4d45ebccac9a8d9c4c6
Registration Date
November 15, 2022
Manufacturer
Authorized Representative

