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Europa Ultra CTO - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Europa Ultra CTO in the Bangladesh medical device market through Pure Global AI's free database. This D medical device is manufactured by RontisCorporationSA in Switzerland. The device was registered on July 03, 2017.

This page provides complete registration details including registration ID (390-5483-017), manufacturer information and country of origin (Switzerland), authorized representative (JMI Hospital Requisite Mfg. Ltd., 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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Bangladesh DGDA Official Data
D
Europa Ultra CTO
Bangladesh Medical Device Registration
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Device Classification
Risk Class
D
Product Name
Europa Ultra CTO
Registration Information
Registration ID
390-5483-017
Registration Date
July 03, 2017
Analysis ID
672c367420e52274bdd9f45fea415494
Manufacturer
Country
Switzerland
Authorized Representative