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cobas z 480 analyzer - FDA Registration 745bd8e23a1e43718fac5c4e5d22a815

Access comprehensive regulatory information for cobas z 480 analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 745bd8e23a1e43718fac5c4e5d22a815 and manufactured by Roche Diagnostics International Ltd. The device was registered on August 02, 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
745bd8e23a1e43718fac5c4e5d22a815
cobas z 480 analyzer
FDA ID: 745bd8e23a1e43718fac5c4e5d22a815
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Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
745bd8e23a1e43718fac5c4e5d22a815
Registration Date
August 02, 2022
Authorized Representative