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9180 Electrolyte Analyzer - FDA Registration 534a8b318421dc2e0857e79e414f909d

Access comprehensive regulatory information for 9180 Electrolyte Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 534a8b318421dc2e0857e79e414f909d and manufactured by Roche Diagnostics International Ltd. The device was registered on September 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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534a8b318421dc2e0857e79e414f909d
9180 Electrolyte Analyzer
FDA ID: 534a8b318421dc2e0857e79e414f909d
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DJ Fang

DJ Fang

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Device Classification
Brand Name
Roche Brand
Registration Information
Analysis ID
534a8b318421dc2e0857e79e414f909d
Registration Date
September 28, 2022
Authorized Representative