Pure Global

Jaruen ureteral stent group - Taiwan Registration 01dd1cf4c9de30f6f5a064ad7e044416

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
01dd1cf4c9de30f6f5a064ad7e044416
Registration Details
Taiwan FDA Registration: 01dd1cf4c9de30f6f5a064ad7e044416
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Jaruen ureteral stent group
TW: ้›…็‰ๆฉ่ผธๅฐฟ็ฎกๆ”ฏๆžถ็ต„
Risk Class 2

Registration Details

01dd1cf4c9de30f6f5a064ad7e044416

DHA05603297509

Company Information

Israel

Product Details

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) โ€ข Pelvic malignancy compressing the ureter โ€ข Inoperable, occlusive, primary or invasive ureteral malignancy โ€ข Ureter-intestinal anastomosis stenosis โ€ข Iatrogenic benign ureteral stenosis

H Gastroenterology and urology

H.4620 Urinary Catheter Stent

import

Dates and Status

Oct 21, 2019

Oct 21, 2029