Pure Global

"Zhaofeng" bone force lumbar intervertebral fusion device - Taiwan Registration a4b9398d7cf4b199e33c998922fb2e24

Access comprehensive regulatory information for "Zhaofeng" bone force 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 a4b9398d7cf4b199e33c998922fb2e24 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
a4b9398d7cf4b199e33c998922fb2e24
Registration Details
Taiwan FDA Registration: a4b9398d7cf4b199e33c998922fb2e24
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Zhaofeng" bone force lumbar intervertebral fusion device
TW: โ€œๅ…†้‹’โ€้ชจๅŠ›่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

a4b9398d7cf4b199e33c998922fb2e24

DHY00500255501

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

Nov 27, 2008

Nov 27, 2013

Aug 10, 2015

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ