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cobas u 411 urine analyzer - FDA Registration 2fd9ac0bf2d081d320f5bb8e113e9ec8

Access comprehensive regulatory information for cobas u 411 urine analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2fd9ac0bf2d081d320f5bb8e113e9ec8 and manufactured by Roche Diagnostics International Ltd. The device was registered on July 28, 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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2fd9ac0bf2d081d320f5bb8e113e9ec8
cobas u 411 urine analyzer
FDA ID: 2fd9ac0bf2d081d320f5bb8e113e9ec8
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Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
2fd9ac0bf2d081d320f5bb8e113e9ec8
Registration Date
July 28, 2022
Authorized Representative