One Step Rapid Test for Syphilis MERISCREEN Syphiline - FDA Registration 52ffc5a5a6612e277948670ae0d4c772
Access comprehensive regulatory information for One Step Rapid Test for Syphilis MERISCREEN Syphiline in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 52ffc5a5a6612e277948670ae0d4c772 and manufactured by Meril Diagnostics Pvt. Ltd.. The device was registered on April 27, 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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52ffc5a5a6612e277948670ae0d4c772
One Step Rapid Test for Syphilis MERISCREEN Syphiline
FDA ID: 52ffc5a5a6612e277948670ae0d4c772
Device Classification
Brand Name
Criteria
Registration Information
Analysis ID
52ffc5a5a6612e277948670ae0d4c772
Registration Date
April 27, 2022
Manufacturer
Authorized Representative

