Singapore HSA registration DE0503688
Teleflex Rusch Ureter Stent Set
Device classification
- Device Class
- CLASS C
- Medical Speciality Area
- Gastroenterology & Urology
Registration information
- Registration Number
- DE0503688
- Registration Date
- October 02, 2019
- Change Notification Approval Date
- March 18, 2024
- Retention Due Date
- October 01, 2025
Product description
Rusch ureter stents are intended for use as routine ureter stents as recommended by a physician or suitably qualified medical personnel. Examples of indications for placement include following ureteric surgery or lithotripsy for ureter stone treatment
Product Owner
- Name
- Teleflex Medical
- Short Name
- Teleflex
- Address
- IDA Business Park, Athlone, Co. Westmeath, IRELAND
Registrant
- Address
- 83 CLEMENCEAU AVENUE, UE SQUARE, #05-05-08, SINGAPORE 239920
Importer
- Address
- 83 CLEMENCEAU AVENUE, UE SQUARE, #05-05-08, SINGAPORE 239920
Model information
- Model Name(s)
- Rüsch Integral Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0 / 9.0) Rüsch Integral Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0 / 9.0) Rüsch Integral Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0 / 9.0) Rüsch Superglide Integral Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0) Rüsch Superglide Integral Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0) Rüsch Superglide Valve DD Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0) Rüsch Superglide Valve DD Ureter Stent Set (Ch. 4.8 / 6.0 / 7.0 / 8.0) Rüsch Superglide Tumour DD Ureter Stent Set (Ch. 7.0) Rüsch Superglide Tumour DD Ureter Stent Set (Ch. 7.0) Rüsch Superglide Tumour DD Ureter Stent Set (Ch. 6.0 / 7.0 / 8.0) Rüsch Superglide Tumour DD Ureter Stent Set (Ch. 6.0 / 7.0 / 8.0)
- Model Identifier(s)
- 334702 334721 334722 334764 334765 335440 335441 335622 335624 335626 335628
About this record
Access comprehensive regulatory information for Teleflex Rusch Ureter Stent Set in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0503688 and owned by Teleflex Medical. The device was registered on October 02, 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 C