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INQWIRE DIAGNOSTIC GUIDEWIRE - Bangladesh Medical Device Registration

Access comprehensive regulatory information for INQWIRE DIAGNOSTIC GUIDEWIRE in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by MeritMedicalIrelandLtd.IrelandforMeritMedicalSystemsInc. in USA. The device was registered on April 23, 2019.

This page provides complete registration details including registration ID (427-6538-019), manufacturer information and country of origin (USA), authorized representative (The Spondon LimitedBSEC Bhaban, (Level-9)102, Kazi Nazrul Islam AvenueKawran Bazar, 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
C
INQWIRE DIAGNOSTIC GUIDEWIRE
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
INQWIRE DIAGNOSTIC GUIDEWIRE
Registration Information
Registration ID
427-6538-019
Registration Date
April 23, 2019
Analysis ID
bb03ecb85902ebb272fa089ae2889b93