Pure Global

"Huayi" guide line - Taiwan Registration 2a3645670807de1d490ab2377fda31e7

Access comprehensive regulatory information for "Huayi" guide line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a3645670807de1d490ab2377fda31e7 and manufactured by HWA YI MEDICAL CO., LTD.. The authorized representative in Taiwan is HWA YI MEDICAL 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
2a3645670807de1d490ab2377fda31e7
Registration Details
Taiwan FDA Registration: 2a3645670807de1d490ab2377fda31e7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Huayi" guide line
TW: โ€œ่ฏๅ„„โ€ๅฐŽๅผ•็ทš
Risk Class 2
Cancelled

Registration Details

2a3645670807de1d490ab2377fda31e7

DHY00500287302

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

Domestic

Dates and Status

Jan 21, 2010

Jan 21, 2015

Aug 21, 2018

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€