Singapore HSA registration DE0506681
JOTEC® E-NSIDE® TAAA Multibranch Stent Graft System
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 description
The E-nside TAAA Multibranch Stent Graft System is indicated for endovascular treatments of patients with thoracoabdominal aortic aneurysms.
Product Owner
- Name
- JOTEC GmbH
- 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
About this record
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.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS D