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Syphilis Rapid Test Strip (Whole Blood/ Serum/ Plasma) - FDA Registration 327a878fe82f9b55a8bfbd1b8b40e55d

Access comprehensive regulatory information for Syphilis Rapid Test Strip (Whole Blood/ Serum/ Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 327a878fe82f9b55a8bfbd1b8b40e55d and manufactured by Hangzhou Biotest Biotech Co., Ltd.. The device was registered on July 01, 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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327a878fe82f9b55a8bfbd1b8b40e55d
Syphilis Rapid Test Strip (Whole Blood/ Serum/ Plasma)
FDA ID: 327a878fe82f9b55a8bfbd1b8b40e55d
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Device Classification
Brand Name
RightSign
Registration Information
Analysis ID
327a878fe82f9b55a8bfbd1b8b40e55d
Registration Date
July 01, 2022
Authorized Representative