Pure Global

TRUEtome 39 CannulatingSphinerotome - Bangladesh Medical Device Registration

Access comprehensive regulatory information for TRUEtome 39 CannulatingSphinerotome in the Bangladesh medical device market through Pure Global AI's free database. This B medical device is manufactured by BostonScientificCorporationUSAMfgr.atBostonScientificCorporation in USA. The device was registered on May 30, 2017.

This page provides complete registration details including registration ID (461-5603-017), manufacturer information and country of origin (USA), authorized representative (Vastec Ltd.,Nurjahan Tower (6th Floor)80/22, Mymensingh Roadm 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.

Free Database
Powered by Pure Global AI
Bangladesh DGDA Official Data
B
TRUEtome 39 CannulatingSphinerotome
Bangladesh Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Risk Class
B
Product Name
TRUEtome 39 CannulatingSphinerotome
Registration Information
Registration ID
461-5603-017
Registration Date
May 30, 2017
Analysis ID
ab4f5ed52dd22e63d65940b12882a228