The Thinprep PAP TEST PreservCyt Solution - FDA Registration 3b40724b4e5b02f978612f266e94fd20
Access comprehensive regulatory information for The Thinprep PAP TEST PreservCyt Solution in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3b40724b4e5b02f978612f266e94fd20 and manufactured by Hologic, Inc.. The device was registered on March 22, 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
3b40724b4e5b02f978612f266e94fd20
The Thinprep PAP TEST PreservCyt Solution
FDA ID: 3b40724b4e5b02f978612f266e94fd20
Device Classification
Brand Name
ThinPrep
Registration Information
Analysis ID
3b40724b4e5b02f978612f266e94fd20
Registration Date
March 22, 2022
Manufacturer
Name
Hologic, Inc.Authorized Representative

