Singapore HSA registration DE0005946
Cordis Disposable Biopsy Forceps
Singapore·CLASS D·Cordis US Corp.·Registered January 14, 2011Device 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 description
Cordis Disposable Biopsy Forceps are indicated for Endomyocardial biopsies allowing to monitor cardiac transplant rejection status and the diagnosis of various cardiac pathologies.
Product Owner
- Name
- Cordis US Corp.
- 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
About this record
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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