JOTEC E-wire Guide Wire - HSA Registration DE0503140
Access comprehensive regulatory information for JOTEC E-wire Guide Wire in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0503140 and owned by JOTEC GmbH. The device was registered on May 24, 2019.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
The E-wire Guide Wire is intended for the placement and replacement of catheters in diagnostic and interventional procedures, particularly for the treatment of abdominal and thoracic aortic aneurysms involving endovascular prostheses.

