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Pureflux

Bangladesh Medical Device Registration · NiproCorporationOdateFactory · Japan · B · Registered May 28, 2016

Device classification
Risk Class
B
Product Name
Pureflux
Registration information
Registration ID
390-4986-015
Registration Date
May 28, 2016
Analysis ID
77c793c41751e3cb531893b9aa4ebfb0
Manufacturer
Name
NiproCorporationOdateFactory
Country
Japan
Authorized representative
Name
JMI Hospital Requisite Mfg. Ltd., Dhaka
About this record

Access comprehensive regulatory information for Pureflux in the Bangladesh medical device market through Pure Global AI's free database. This B medical device is manufactured by NiproCorporationOdateFactory in Japan. The device was registered on May 28, 2016.

This page provides complete registration details including registration ID (390-4986-015), manufacturer information and country of origin (Japan), 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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