One Step Syphilis Rapid Test Cassette (WB/Serum/Plasma) - FDA Registration 60e1984dd16c0ebaf8d68f87167b6194
Access comprehensive regulatory information for One Step Syphilis Rapid Test Cassette (WB/Serum/Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 60e1984dd16c0ebaf8d68f87167b6194 and manufactured by Nantong Diagnos Biotechnology Co., Ltd. The device was registered on August 25, 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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60e1984dd16c0ebaf8d68f87167b6194
One Step Syphilis Rapid Test Cassette (WB/Serum/Plasma)
FDA ID: 60e1984dd16c0ebaf8d68f87167b6194
Device Classification
Brand Name
DIAGNOSIS
Registration Information
Analysis ID
60e1984dd16c0ebaf8d68f87167b6194
Registration Date
August 25, 2022
Manufacturer
Authorized Representative

