Pure Global

"Zhaofeng" Weizhou polymer material lumbar intervertebral fusion device - Taiwan Registration 3c213ed19a0041008d99a00be24f2536

Access comprehensive regulatory information for "Zhaofeng" Weizhou polymer material lumbar intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3c213ed19a0041008d99a00be24f2536 and manufactured by Zhaofeng Biotech Co., Ltd.;; Guanya International Technology Co., Ltd. The authorized representative in Taiwan is Zhaofeng Biotechnology 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
3c213ed19a0041008d99a00be24f2536
Registration Details
Taiwan FDA Registration: 3c213ed19a0041008d99a00be24f2536
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Zhaofeng" Weizhou polymer material lumbar intervertebral fusion device
TW: โ€œๅ…†้‹’โ€ๅจๆ‹“้ซ˜ๅˆ†ๅญๆๆ–™่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

3c213ed19a0041008d99a00be24f2536

DHY00500250802

Company Information

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

Domestic

Dates and Status

Sep 25, 2008

Sep 25, 2013

Aug 10, 2015

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ