Israel Ministry of Health registration 24820057
Powerplex Pro
Local name: פאוארפלקס פרו
Device classification
- Product Type
- radiology
Registration information
- Analysis ID
- 24820057
- Registration Date
- December 31, 2022
Manufacturer
- Country
- USA
Authorized Representative
About this record
Access comprehensive regulatory information for Powerplex Pro in the Israel medical device market through Pure Global AI's free database. This medical device is registered under Ministry of Health ID 24820057 and manufactured by Cordis Corporation. The device was registered on December 31, 2022.
This page provides complete registration details including product type (radiology), 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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