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LOGIQ Ultrasound System(LOGIQ V3, V5, V5 Expert) - Bangladesh Medical Device Registration

Access comprehensive regulatory information for LOGIQ Ultrasound System(LOGIQ V3, V5, V5 Expert) in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by GEMedicalSystems(China)Co.Ltd.No.19ChangjiangRoadWuXiNationalHi-techDevelopmentZoneJiangsu in China. The device was registered on December 06, 2018.

This page provides complete registration details including registration ID (457-6206-018), manufacturer information and country of origin (China), authorized representative (GE Healthcare Banglades Ltd.OS 1401-1402, Level 14, Shanta WesternTower,186, Tejgaon l/A, 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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LOGIQ Ultrasound System(LOGIQ V3, V5, V5 Expert)
Bangladesh Medical Device Registration
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DJ Fang

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Device Classification
Risk Class
C
Product Name
LOGIQ Ultrasound System(LOGIQ V3, V5, V5 Expert)
Registration Information
Registration ID
457-6206-018
Registration Date
December 06, 2018
Analysis ID
6d8151f7b99416c8f7c7f922751f99a8