careHPV Test Controller - FDA Registration 20c9989859522b8d23f547496f687190
Access comprehensive regulatory information for careHPV Test Controller in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 20c9989859522b8d23f547496f687190 and manufactured by Plexus Manufacturing Sdn Bhd. The device was registered on November 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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FDA Official Data
20c9989859522b8d23f547496f687190
careHPV Test Controller
FDA ID: 20c9989859522b8d23f547496f687190
Device Classification
Brand Name
QIAGEN
Registration Information
Analysis ID
20c9989859522b8d23f547496f687190
Registration Date
November 25, 2022
Manufacturer
Authorized Representative

