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CRP Turbilatex - FDA Registration bb5b2f1f897a66b62ee0f82686e674a3

Access comprehensive regulatory information for CRP Turbilatex in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID bb5b2f1f897a66b62ee0f82686e674a3 and manufactured by BEACON DIAGNOSTICS PVT.LTD.. The device was registered on October 08, 2021.

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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bb5b2f1f897a66b62ee0f82686e674a3
CRP Turbilatex
FDA ID: bb5b2f1f897a66b62ee0f82686e674a3
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DJ Fang

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Device Classification
Brand Name
BEACON Brand
Registration Information
Analysis ID
bb5b2f1f897a66b62ee0f82686e674a3
Registration Date
October 08, 2021
Authorized Representative