Syphilis Ab Rapid Test - FDA Registration 8193de148eacbd6ba4cadabc384c2293
Access comprehensive regulatory information for Syphilis Ab Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8193de148eacbd6ba4cadabc384c2293 and manufactured by CTK Biotech, Inc.. The device was registered on October 07, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
8193de148eacbd6ba4cadabc384c2293
Syphilis Ab Rapid Test
FDA ID: 8193de148eacbd6ba4cadabc384c2293
Device Classification
Brand Name
Onsite
Registration Information
Analysis ID
8193de148eacbd6ba4cadabc384c2293
Registration Date
October 07, 2022
Manufacturer
Authorized Representative

