Pure Global

"Nanwei Medicine" three-stage dilated balloon catheter - Taiwan Registration 3edaab7f1a1075bb86dc9ee0fd4a0c0f

Access comprehensive regulatory information for "Nanwei Medicine" three-stage dilated balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3edaab7f1a1075bb86dc9ee0fd4a0c0f and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is AP Biotech Co., Ltd.

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
3edaab7f1a1075bb86dc9ee0fd4a0c0f
Registration Details
Taiwan FDA Registration: 3edaab7f1a1075bb86dc9ee0fd4a0c0f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Nanwei Medicine" three-stage dilated balloon catheter
TW: โ€œๅ—ๅพฎ้†ซๅญธโ€ไธ‰ๆฎตๆ“ดๅผตๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 2

Registration Details

3edaab7f1a1075bb86dc9ee0fd4a0c0f

DHA09200090901

Company Information

Product Details

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

H Gastroenterology and urology

H.5365 Esophageal extenders

Input;; Chinese goods

Dates and Status

Jan 12, 2018

Jan 12, 2028