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Cerebase DA Guide Sheath - Bangladesh Medical Device Registration

Access comprehensive regulatory information for Cerebase DA Guide Sheath in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by MedosInternationalSarlSwitzerland.ManufacturingSite:CerenovusInc. in Mexico. The device was registered on September 14, 2023.

This page provides complete registration details including registration ID (575-8748-2023), manufacturer information and country of origin (Mexico), authorized representative (Refresh Medical Device, House-452, (3rd Floor), Apollo Link Road, Solmaid Vatara, dhaka, Bangladesh), 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
Cerebase DA Guide Sheath
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
Cerebase DA Guide Sheath
Registration Information
Registration ID
575-8748-2023
Registration Date
September 14, 2023
Analysis ID
f1408c6ec8407fc96cb8f2e80ff850c1