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Cobas 4800 MRSA/SA Controls and Cofactor Kit - FDA Registration 6e0df347a8411835f8b597c99382f5bd

Access comprehensive regulatory information for Cobas 4800 MRSA/SA Controls and Cofactor Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6e0df347a8411835f8b597c99382f5bd 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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6e0df347a8411835f8b597c99382f5bd
Cobas 4800 MRSA/SA Controls and Cofactor Kit
FDA ID: 6e0df347a8411835f8b597c99382f5bd
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Device Classification
Brand Name
ROCHE
Registration Information
Analysis ID
6e0df347a8411835f8b597c99382f5bd
Registration Date
November 29, 2022
Authorized Representative