Lysercell WDF - FDA Registration 6e7af70738349c1996ad0e13853fb7e9
Access comprehensive regulatory information for Lysercell WDF in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6e7af70738349c1996ad0e13853fb7e9 and manufactured by Sysmex Asia Pacific Pte Ltd.. The device was registered on December 14, 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
6e7af70738349c1996ad0e13853fb7e9
Lysercell WDF
FDA ID: 6e7af70738349c1996ad0e13853fb7e9
Device Classification
Brand Name
Sysmex
Registration Information
Analysis ID
6e7af70738349c1996ad0e13853fb7e9
Registration Date
December 14, 2022
Manufacturer
Authorized Representative

