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Cobas 4800 HPV Amplification/Detection Kit - FDA Registration 0bf89091c35406679a2bdc5b80ccc8f6

Access comprehensive regulatory information for Cobas 4800 HPV Amplification/Detection Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0bf89091c35406679a2bdc5b80ccc8f6 and manufactured by Roche Molecular Systems, Inc.. The device was registered on November 29, 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
0bf89091c35406679a2bdc5b80ccc8f6
Cobas 4800 HPV Amplification/Detection Kit
FDA ID: 0bf89091c35406679a2bdc5b80ccc8f6
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Device Classification
Brand Name
Roche
Registration Information
Analysis ID
0bf89091c35406679a2bdc5b80ccc8f6
Registration Date
November 29, 2022
Authorized Representative