Pure Global

"Nishibi" electric hemostatic device - Taiwan Registration a0fe3523b74ad1e7af05bec3d495e38a

Access comprehensive regulatory information for "Nishibi" electric hemostatic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0fe3523b74ad1e7af05bec3d495e38a and manufactured by ZIMMER SURGICAL,INC.. The authorized representative in Taiwan is Taiwan Zimmer Medical Device 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
a0fe3523b74ad1e7af05bec3d495e38a
Registration Details
Taiwan FDA Registration: a0fe3523b74ad1e7af05bec3d495e38a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Nishibi" electric hemostatic device
TW: "่ฅฟ็พŽ" ้›ปๅ‹•ๆญข่ก€ๅ™จ
Risk Class 2
Cancelled

Registration Details

a0fe3523b74ad1e7af05bec3d495e38a

DHA00601119206

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Apr 13, 2005

Apr 13, 2015

Jun 25, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ