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Glidsheath Slender - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Glidsheath Slender in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by AshitakaFactoryofTerumoCorporation in Japan. The device was registered on January 31, 2018.

This page provides complete registration details including registration ID (465-5986-018), manufacturer information and country of origin (Japan), authorized representative (M/s. UniMed Ltd), 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
Glidsheath Slender
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
Glidsheath Slender
Registration Information
Registration ID
465-5986-018
Registration Date
January 31, 2018
Analysis ID
9d151cff6cc07c977920ba2de8d082ae
Manufacturer
Authorized Representative