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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.

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CLASS B
DE0503140
JOTEC E-wire Guide Wire
HSA Registration Number: DE0503140
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Product Description

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.

Device Classification
Device Class
CLASS B
Medical Speciality Area
General & Plastic Surgery
Registration Information
Registration Number
DE0503140
Registration Date
May 24, 2019
Retention Due Date
May 23, 2025
Product Owner
Short Name
JOTEC GmbH
Address
Lotzenacker 23, 72379 Hechingen, GERMANY
Registrant
Address
1 MARINA BOULEVARD, ONE MARINA BOULEVARD, #28-00, SINGAPORE 018989
Importer
Address
12A JALAN AMPAS, BALESTIER WAREHOUSE BUILDING, #03-03, SINGAPORE 329516
Model Information
Model Name(s)
E-wire Guide Wire E-wire Guide Wire
Model Identifier(s)
76XX1935N-06 76XX3035N-06