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Ankura CUFF Stent Graft System - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Ankura CUFF Stent Graft System in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by LifetechScientific(Europe)CorporationU.A in Netherlands. The device was registered on September 18, 2022.

This page provides complete registration details including registration ID (711-8425-2022), manufacturer information and country of origin (Netherlands), authorized representative (Bangladesh Healthcare & Pharma Solutiuon205/1, Maddha Paikpara, Mirpur, Dhaka), 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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Ankura CUFF Stent Graft System
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
Ankura CUFF Stent Graft System
Registration Information
Registration ID
711-8425-2022
Registration Date
September 18, 2022
Analysis ID
8c53ffcd53c45ec1e8ffb9f7439782e8