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Percuflex Plus Ureteral Stent - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Percuflex Plus Ureteral Stent in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by BostonScientificCorporationCostaRicaforBostonScientificCorporation in USA. The device was registered on March 09, 2020.

This page provides complete registration details including registration ID (513-6854-2020), manufacturer information and country of origin (USA), authorized representative (M/s. Globex Marketing Co. Ltd. R. H. Home Centre (6th Floor)74/B/1, Green Road, 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
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Percuflex Plus Ureteral Stent
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
Percuflex Plus Ureteral Stent
Registration Information
Registration ID
513-6854-2020
Registration Date
March 09, 2020
Analysis ID
ac2560cb370bf61e8e34904dfdc167b3