Taiwan FDA registration 01dd1cf4c9de30f6f5a064ad7e044416
Jaruen ureteral stent group
TW: 雅琉恩輸尿管支架組
Taiwan·Risk Class 2·Allium Ltd.·Registered Oct 21, 2019 – Oct 21, 2029ActiveRegistration details
- Analysis ID
- 01dd1cf4c9de30f6f5a064ad7e044416
- Customs Code
- DHA05603297509
Company information
- Manufacturer
- Allium Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- HUILI MEDICAL EQUIPMENT LIMITED
Product details
- Intended Use
- URS is indicated for malignant or benign ureteral obstruction and long-term ureteral stent use is necessary (especially if patients have a double J stent inserted for at least 6 months or more) • Pelvic malignancy compressing the ureter • Inoperable, occlusive, primary or invasive ureteral malignancy • Ureter-intestinal anastomosis stenosis • Iatrogenic benign ureteral stenosis
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.4620 Urinary Catheter Stent
- Import Information
- import
Dates and status
- Registration Date
- Oct 21, 2019
- Expiry Date
- Oct 21, 2029
About this record
Access comprehensive regulatory information for Jaruen ureteral stent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01dd1cf4c9de30f6f5a064ad7e044416 and manufactured by Allium Ltd.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.
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