Smart Flex - Peripheral stent - Ministry of Health Registration 24820052
Access comprehensive regulatory information for Smart Flex - Peripheral stent in the Israel medical device market through Pure Global AI's free database. This medical device is registered under Ministry of Health ID 24820052 and manufactured by Cordis Cashel. The device was registered on July 31, 2022.
This page provides complete registration details including product type (Cardiology), manufacturer information, and regulatory compliance data from the official Israel Ministry of Health medical device database. Pure Global AI offers free access to Israel's complete medical device registry.
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Ministry of Health Official Data
24820052
Smart Flex - Peripheral stent
Ministry of Health ID: 24820052
Local name: 住诪讗专讟 驻诇拽住 - 转讜诪讻讜谉 (住讟谞讟) 驻专讬驻专讬讗诇讬
Device Classification
Product Type
Cardiology
Registration Information
Analysis ID
24820052
Registration Date
July 31, 2022
Manufacturer
Name
Cordis CashelCountry
IRELAND

