Singapore HSA registration DE0007241
Argon Jawz Endomyocardial Biopsy Forcep
Device classification
- Device Class
- CLASS D
- Medical Speciality Area
- Cardiovascular
Registration information
- Registration Number
- DE0007241
- Registration Date
- July 08, 2011
- Change Notification Approval Date
- March 05, 2024
- Retention Due Date
- July 07, 2025
Product description
The 50cm and 70cm Disposable Radiopaque Endomyocardial Biopsy Forceps are designed for Right Ventricular Biopsies using the Jugular Approach, and for Right or Left Ventricular Pediatric Biopsies using the Femoral Approach. The 105cm Disposable Radiopaque Endomyocardial Biopsy Forceps are designed for Right or Left Ventricular Biopsies using the Femoral Approach.
Product Owner
- Short Name
- Argon Medical Device
- Address
- 1445 Flat Creek Road Athens, Texas 75751, UNITED STATES
Registrant
- Address
- 5 JALAN KILANG BARAT, PETRO CENTRE, #09-05, SINGAPORE 159349
Importer
- Address
- 5 JALAN KILANG BARAT, PETRO CENTRE, #09-00, SINGAPORE 159349
Model information
- Model Name(s)
- Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep Jawz Endomyocardial Biopsy Forcep
- Model Identifier(s)
- 190020 190030 190031 190040 190051 190060 190065 190066 190070 190075 190080 190081 190085 190086 190090 190095
About this record
Access comprehensive regulatory information for Argon Jawz Endomyocardial Biopsy Forcep in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0007241 and owned by Argon Medical Devices, Inc. The device was registered on July 08, 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.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS D