STANDARD F β-hCG FIA - FDA Registration 46f8ac9d8dac7c157efbd04a0b3e2e96
Access comprehensive regulatory information for STANDARD F β-hCG FIA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 46f8ac9d8dac7c157efbd04a0b3e2e96 and manufactured by SD Biosensor, Inc.. The device was registered on October 19, 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
46f8ac9d8dac7c157efbd04a0b3e2e96
STANDARD F β-hCG FIA
FDA ID: 46f8ac9d8dac7c157efbd04a0b3e2e96
Device Classification
Brand Name
STANDARD F
Registration Information
Analysis ID
46f8ac9d8dac7c157efbd04a0b3e2e96
Registration Date
October 19, 2022
Manufacturer
Authorized Representative

