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Anti-Human Globulin Polyspecific AHG for Coombs Test - FDA Registration 2755f7fcc8020e94bb60391c7de5eba7

Access comprehensive regulatory information for Anti-Human Globulin Polyspecific AHG for Coombs Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2755f7fcc8020e94bb60391c7de5eba7 and manufactured by Rapid Labs Limited. The device was registered on September 27, 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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2755f7fcc8020e94bb60391c7de5eba7
Anti-Human Globulin Polyspecific AHG for Coombs Test
FDA ID: 2755f7fcc8020e94bb60391c7de5eba7
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Device Classification
Brand Name
Rapid Labs
Registration Information
Analysis ID
2755f7fcc8020e94bb60391c7de5eba7
Registration Date
September 27, 2022
Manufacturer
Authorized Representative