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Rejimed Plastic Blood Bag for single use - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Rejimed Plastic Blood Bag for single use 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 single use
Bangladesh Medical Device Registration
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Device Classification
Risk Class
B
Product Name
Rejimed Plastic Blood Bag for single use
Registration Information
Registration ID
33-8462-2022
Registration Date
December 10, 2022
Analysis ID
b418eab9d4fa066af2771cb21eeb60c7