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LIQUID ASSAYED SPECIFIC PROTEIN - CONTROL LEVEL 3 (SP CONTROL 3) - FDA Registration 2025c02bb5b880e3e4ac44cba6611584

Access comprehensive regulatory information for LIQUID ASSAYED SPECIFIC PROTEIN - CONTROL LEVEL 3 (SP CONTROL 3) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2025c02bb5b880e3e4ac44cba6611584 and manufactured by Randox Laboratories Ltd.. The device was registered on April 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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2025c02bb5b880e3e4ac44cba6611584
LIQUID ASSAYED SPECIFIC PROTEIN - CONTROL LEVEL 3 (SP CONTROL 3)
FDA ID: 2025c02bb5b880e3e4ac44cba6611584
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Device Classification
Brand Name
Randox
Registration Information
Analysis ID
2025c02bb5b880e3e4ac44cba6611584
Registration Date
April 28, 2022
Manufacturer
Authorized Representative