Israel Ministry of Health registration 980433
Troflex and Imogard
Local name: טרופלקס ואימוגארד
Device classification
- Product Type
- laboratory
Registration information
- Analysis ID
- 980433
- Registration Date
- August 31, 2023
Manufacturer
- Country
- JAPAN
Authorized Representative
About this record
Access comprehensive regulatory information for Troflex and Imogard in the Israel medical device market through Pure Global AI's free database. This medical device is registered under Ministry of Health ID 980433 and manufactured by Terumo Corporation. The device was registered on August 31, 2023.
This page provides complete registration details including product type (laboratory), 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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