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Focusforce - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Focusforce in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by ValeantMedSp.Z.o.o.ulRyzowa3102-495Warszawa in Poland. The device was registered on April 26, 2017.

This page provides complete registration details including registration ID (487-5558-017), manufacturer information and country of origin (Poland), authorized representative (Janata Traders, 62/2, Purana Paltan (1stFloor), Dhaka-1000), risk classification, and regulatory compliance data from the official Bangladesh medical device database. Pure Global AI offers free access to Bangladesh DGDA's medical device registry, helping global MedTech companies navigate Bangladesh regulations efficiently.

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Bangladesh DGDA Official Data
C
Focusforce
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
Focusforce
Registration Information
Registration ID
487-5558-017
Registration Date
April 26, 2017
Analysis ID
9f5c20820c5ee6e953ed1f4747084bcc