Pure Global

Allium Biliary Stent(BIS) System - Taiwan Registration 38ab3dc2e650a0223f2e1644af24b506

Access comprehensive regulatory information for Allium Biliary Stent(BIS) System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38ab3dc2e650a0223f2e1644af24b506 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
38ab3dc2e650a0223f2e1644af24b506
Registration Details
Taiwan FDA Registration: 38ab3dc2e650a0223f2e1644af24b506
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Allium Biliary Stent(BIS) System
TW: ้›…็‰ๆฉ่†ฝ็ฎกๆ”ฏๆžถ็ต„
Risk Class 2
MD

Registration Details

38ab3dc2e650a0223f2e1644af24b506

Ministry of Health Medical Device Import No. 030597

DHA05603059706

Company Information

Israel

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H5010 Bile ductal catheters and their accessories

Imported from abroad

Dates and Status

Dec 15, 2017

Dec 15, 2027