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JOTEC® E-NSIDE® TAAA Multibranch Stent Graft System - HSA Registration DE0506681

Access comprehensive regulatory information for JOTEC® E-NSIDE® TAAA Multibranch Stent Graft System in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0506681 and owned by JOTEC GmbH. The device was registered on February 28, 2022.

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 D
DE0506681
JOTEC® E-NSIDE® TAAA Multibranch Stent Graft System
HSA Registration Number: DE0506681
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Product Description

The E-nside TAAA Multibranch Stent Graft System is indicated for endovascular treatments of patients with thoracoabdominal aortic aneurysms.

Device Classification
Device Class
CLASS D
Medical Speciality Area
Cardiovascular
Registration Information
Registration Number
DE0506681
Registration Date
February 28, 2022
Retention Due Date
February 27, 2026
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-nside TAAA Multibranch Stent Graft System E-nside TAAA Multibranch Stent Graft System E-nside TAAA Multibranch Stent Graft System E-nside TAAA Multibranch Stent Graft System
Model Identifier(s)
65MU332621-4B8866-00 65MU333021-4B8866-00 65MU382621-4B8866-00 65MU383021-4B8866-00