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STANDARD F CRP and STANDARD F hs-CRP - FDA Registration afe08a7f4d9f5d23d6faecd81881cd70

Access comprehensive regulatory information for STANDARD F CRP and STANDARD F hs-CRP in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID afe08a7f4d9f5d23d6faecd81881cd70 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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afe08a7f4d9f5d23d6faecd81881cd70
STANDARD F CRP and STANDARD F hs-CRP
FDA ID: afe08a7f4d9f5d23d6faecd81881cd70
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Device Classification
Brand Name
STANDARD F
Registration Information
Analysis ID
afe08a7f4d9f5d23d6faecd81881cd70
Registration Date
October 19, 2022
Manufacturer
Authorized Representative