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R.P.R (VDRL TEST) KIT - FDA Registration bb75e509074b9a077cc0941163385710

Access comprehensive regulatory information for R.P.R (VDRL TEST) KIT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID bb75e509074b9a077cc0941163385710 and manufactured by Biolab Diagnostics (I) Pvt. Ltd. The device was registered on November 26, 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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bb75e509074b9a077cc0941163385710
R.P.R (VDRL TEST) KIT
FDA ID: bb75e509074b9a077cc0941163385710
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Device Classification
Brand Name
Biolab Diagnostics
Registration Information
Analysis ID
bb75e509074b9a077cc0941163385710
Registration Date
November 26, 2022
Authorized Representative