Singapore HSA registration DE0003621
Cordis ANGIOGUARD™ RX Emboli Capture Guidewire System
Device classification
- Device Class
- CLASS D
- Medical Speciality Area
- General & Plastic Surgery
- HSA Product Code
- HSAMDD00110
- HS Code
- 90189090
Registration information
- Registration Number
- DE0003621
- Registration Date
- June 08, 2006
- Change Notification Approval Date
- September 18, 2024
- Retention Due Date
- August 09, 2025
Product description
Intended for coronary, carotid, and peripheral uses to facilitate the placement of diagnostic and interventional devices, and capture emboli, thereby reducing the risk of embolization, during procedures.
Product Owner
- Short Name
- Cordis
- Address
- 14201 North West 60th Avenue, Miami Lakes, Florida 33014, UNITED STATES
Registrant
- Address
- 600 NORTH BRIDGE ROAD, PARKVIEW SQUARE, #05-01, SINGAPORE 188778
Importer
- Address
- 5 TAI SENG DRIVE, SCA CREATIVE CENTRE, #02-01, SINGAPORE 535217 15 CHANGI NORTH WAY, #01-00, SINGAPORE 498770
Model information
- Model Name(s)
- ANGIOGUARD™ RX Extra SupportEmboli Capture Guidewire System ANGIOGUARD™ RX Medium Support Emboli Capture Guidewire System ANGIOGUARD™ RX Extra SupportEmboli Capture Guidewire System ANGIOGUARD™ RX Medium Support Emboli Capture Guidewire System ANGIOGUARD™ RX Extra SupportEmboli Capture Guidewire System ANGIOGUARD™ RX Medium Support Emboli Capture Guidewire System ANGIOGUARD™ RX Extra SupportEmboli Capture Guidewire System ANGIOGUARD™ RX Medium Support Emboli Capture Guidewire System ANGIOGUARD™ RX Extra SupportEmboli Capture Guidewire System ANGIOGUARD™ RX Medium Support Emboli Capture Guidewire System
- Model Identifier(s)
- 401814RE 401814RM 501814RE 501814RM 601814RE 601814RM 701814RE 701814RM 801814RE 801814RM
About this record
Access comprehensive regulatory information for Cordis ANGIOGUARD™ RX Emboli Capture Guidewire 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 DE0003621 and owned by Cordis Corporation. The device was registered on June 08, 2006.
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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