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Rejimed Plastic Blood Bag for singleuse - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Rejimed Plastic Blood Bag for singleuse in the Bangladesh medical device market through Pure Global AI's free database. This B medical device is manufactured by SuzhouLaishiTransfusionEquipmentCo.Ltd.ChangshengRoadTongliTownWujiangDistrictSuzhouCityJiangsuProvince in China. The device was registered on December 10, 2022.

This page provides complete registration details including registration ID (33-8462-2022), manufacturer information and country of origin (China), authorized representative (Rejimed International (Pvt) Ltd., House-330,South Paikpara, Mirpur, Dhaka-1216), 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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Rejimed Plastic Blood Bag for singleuse
Bangladesh Medical Device Registration
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Device Classification
Risk Class
B
Product Name
Rejimed Plastic Blood Bag for singleuse
Registration Information
Registration ID
33-8462-2022
Registration Date
December 10, 2022
Analysis ID
3390e1ccb814da9ef6a2bd2658467f78