Pure Global

"Difu Spine" titanium intervertebral fixation mesh - Taiwan Registration 4431711dd7192fdbf7916262db258620

Access comprehensive regulatory information for "Difu Spine" titanium intervertebral fixation mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4431711dd7192fdbf7916262db258620 and manufactured by DEPUY SPINE, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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
4431711dd7192fdbf7916262db258620
Registration Details
Taiwan FDA Registration: 4431711dd7192fdbf7916262db258620
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Difu Spine" titanium intervertebral fixation mesh
TW: "ๅธๅฏŒ่„ŠๆคŽ" ้ˆฆ่ณชๆคŽ้–“ๅ›บๅฎš็ถฒ
Risk Class 2
Cancelled

Registration Details

4431711dd7192fdbf7916262db258620

DHA00601012907

Company Information

United States

Product Details

Vacuum.

N Orthopedics

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

import

Dates and Status

Nov 08, 2002

Nov 08, 2017

Nov 04, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ