Singapore HSA registration DE0503213
Terumo Surshield Surflash PS Safety I.V Catheter
Singapore·CLASS B·TERUMO CORPORATION·Registered June 06, 2019Device classification
- Device Class
- CLASS B
- Medical Speciality Area
- General Hospital
Registration information
- Registration Number
- DE0503213
- Registration Date
- June 06, 2019
- Change Notification Approval Date
- March 27, 2023
- Retention Due Date
- June 05, 2025
Product description
The Surshield Surflash PS Safety I.V Catheter is inserted into the patient’s vascular system for short term use to withdraw blood samples, administer fluid intravenously, or monitor blood pressure by attaching a monitoring line. The needle shield feature aids in the prevention of needle stick injuries. These catheters may be used for any patient population with consideration given to adequacy of vascular anatomy and appropriateness for the solution being infused and duration of therapy
Product Owner
- Short Name
- TERUMO CORPORATION
- Address
- 2-44-1, Hatagaya, Shibuya-ku, Tokyo, 151-0072, JAPAN
Registrant
- Address
- 300 BEACH ROAD, THE CONCOURSE, #37-01, SINGAPORE 199555
Importer
- Address
- 300 BEACH ROAD, CONCOURSE, THE, #37-01, SINGAPORE 199555 300 BEACH ROAD, CONCOURSE, THE, #33-06, SINGAPORE 199555
Model information
- Model Name(s)
- Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter Surshield Surflash PS Safety I.V Catheter
- Model Identifier(s)
- SR*SFF1832 SR*SFF1851 SR*SFF2025 SR*SFF2032 SR*SFF2051 SR*SFF2225 SR*SFF2232 SR*SFF2419
About this record
Access comprehensive regulatory information for Terumo Surshield Surflash PS Safety I.V Catheter in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0503213 and owned by TERUMO CORPORATION. The device was registered on June 06, 2019.
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