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Cordis Disposable Biopsy Forceps - HSA Registration DE0005946

Access comprehensive regulatory information for Cordis Disposable Biopsy Forceps in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0005946 and owned by Cordis US Corp.. The device was registered on January 14, 2011.

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
DE0005946
Cordis Disposable Biopsy Forceps
HSA Registration Number: DE0005946
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Product Description

Cordis Disposable Biopsy Forceps are indicated for Endomyocardial biopsies allowing to monitor cardiac transplant rejection status and the diagnosis of various cardiac pathologies.

Device Classification
Device Class
CLASS D
Medical Speciality Area
General Hospital
Registration Information
Registration Number
DE0005946
Registration Date
January 14, 2011
Change Notification Approval Date
June 06, 2024
Retention Due Date
January 13, 2026
Product Owner
Short Name
Cordis US Corp.
Address
14201 North West 60th Avenue, Miami Lakes, Florida 33014, Florida, 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)
Biopsy Forceps Biopsy Forceps Biopsy Forceps Biopsy Forceps
Model Identifier(s)
504300 504300L 504302 504302L