Singapore HSA registration DE0506623
Verathon GlideScope® BFlex 3.8 Single-Use Bronchoscope
Device classification
- Device Class
- CLASS B
- Medical Speciality Area
- Ear, Nose & Throat
Registration information
- Registration Number
- DE0506623
- Registration Date
- February 03, 2022
- Retention Due Date
- February 02, 2026
Product description
GlideScope BFlex Single-Use bronchoscopes are intended to work with a video monitor, in conjunction with non-powered endoscopic accessories and other ancillary equipment, for endoscopy within the airways and tracheobronchial tree.
Product Owner
- Short Name
- Verathon Medical Canada ULC
- Address
- 2227 Douglas Rd Burnaby,, BC V5C 5A9, CANADA
Registrant
- Address
- 11 LORONG 3 TOA PAYOH, BLOCK B JACKSON SQUARE, #01-13, SINGAPORE 319579
Importer
- Address
- 11 LORONG 3 TOA PAYOH, JACKSON SQUARE, #01-13, SINGAPORE 319579 11 LORONG 3 TOA PAYOH, JACKSON SQUARE, #01-13, SINGAPORE 319579
Model information
- Model Name(s)
- GlideScope® Core 10 Premium Configuration with Smart Cable and GlideScope® QuickConnect Cable GlideScope® Core 10 Premium Configuration with GlideScope® QuickConnect Cable GlideScope® Core 10 Monitor Kit GlideScope® Core 15 Premium Configuration with Smart Cable and GlideScope® QuickConnect Cable GlideScope® Core 15 Premium Configuration with GlideScope® QuickConnect Cable GlideScope® Core 15 Monitor Kit GlideScope® Video Monitor GlideScope® Core 10 Monitor GlideScope® BFlex 3.8 Single-Use Flexible Bronchoscope GlideScope® BFlex 3.8 Single-Use Flexible Bronchoscope, Qty. 5 GlideScope® Core 15 Monitor
- Model Identifier(s)
- 0270-0991 0270-0995 0270-0996 0270-1022 0270-1030 0270-1033 0570-0338 0570-0376 0570-0380 0570-0396 0570-0404
About this record
Access comprehensive regulatory information for Verathon GlideScope® BFlex 3.8 Single-Use Bronchoscope in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0506623 and owned by Verathon Medical Canada ULC. The device was registered on February 03, 2022.
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 B