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Cordis OPTEASE™ Retrieval Catheter - HSA Registration DE0004240

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.

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CLASS D
DE0004240
Cordis OPTEASE™ Retrieval Catheter
HSA Registration Number: DE0004240
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Product Description

Indicated for the retrieval of the Cordis OPTEASE™ Retrievable Vena Cava Filter from the inferior vena cava.

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 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