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Elite 580 Hematology Analyser - FDA Registration 5fb305bbc91e4bc5411ab3758fd4b3d4

Access comprehensive regulatory information for Elite 580 Hematology Analyser in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5fb305bbc91e4bc5411ab3758fd4b3d4 and manufactured by Erba Lachema s.r.o. The device was registered on May 18, 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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5fb305bbc91e4bc5411ab3758fd4b3d4
Elite 580 Hematology Analyser
FDA ID: 5fb305bbc91e4bc5411ab3758fd4b3d4
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Device Classification
Brand Name
Grass Mannheim
Registration Information
Analysis ID
5fb305bbc91e4bc5411ab3758fd4b3d4
Registration Date
May 18, 2022
Manufacturer
Authorized Representative