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HI-TORQUE IntermediateGuideware - Bangladesh Medical Device Registration

Access comprehensive regulatory information for HI-TORQUE IntermediateGuideware in the Bangladesh medical device market through Pure Global AI's free database. This D medical device is manufactured by AbbottVascular3200LakesideDriveSantaClaraCalifornia in USA. The device was registered on May 28, 2018.

This page provides complete registration details including registration ID (401-6190-018), manufacturer information and country of origin (USA), authorized representative (Cardiac Care LimitedZahir Mansion 476/C MalibaghDIT Road (3rd Floor) 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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HI-TORQUE IntermediateGuideware
Bangladesh Medical Device Registration
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Device Classification
Risk Class
D
Product Name
HI-TORQUE IntermediateGuideware
Registration Information
Registration ID
401-6190-018
Registration Date
May 28, 2018
Analysis ID
0586d29acc05514309b9e0a853892d94