Singapore HSA registration DE0004240
Cordis OPTEASE™ Retrieval Catheter
Device classification
- Device Class
- CLASS D
- Medical Speciality Area
- Cardiovascular
- HSA Product Code
- HSAMDD00110
- HS Code
- 90183910
Registration information
- Registration Number
- DE0004240
- Registration Date
- April 28, 2008
- Change Notification Approval Date
- June 06, 2024
- Retention Due Date
- August 09, 2025
Product description
Indicated for the retrieval of the Cordis OPTEASE™ Retrievable Vena Cava Filter from the inferior vena cava.
Product Owner
- Short Name
- Cordis
- Address
- 14201 N.W. 60th Avenue, Miami Lakes,, Florida 33014, UNITED STATES
Registrant
- Address
- 600 NORTH BRIDGE ROAD, PARKVIEW SQUARE, #05-01, SINGAPORE 188778
Importer
- Address
- 10 KALLANG AVENUE, APERIA, #10-10/18, SINGAPORE 339510 15 CHANGI NORTH WAY, #01-00, SINGAPORE 498770
Model information
- Model Name(s)
- OptEase™ Retrieval Catheter
- Model Identifier(s)
- 466-C210F
About this record
Access comprehensive regulatory information for Cordis OPTEASE™ Retrieval Catheter in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0004240 and owned by Cordis Corporation. The device was registered on April 28, 2008.
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