Pure Global

"Medtronic" Siddy percutaneous spinal fixation system - Taiwan Registration c7de9b4bf85928ab9e74f859d195a06e

Access comprehensive regulatory information for "Medtronic" Siddy percutaneous spinal fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c7de9b4bf85928ab9e74f859d195a06e and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (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
c7de9b4bf85928ab9e74f859d195a06e
Registration Details
Taiwan FDA Registration: c7de9b4bf85928ab9e74f859d195a06e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" Siddy percutaneous spinal fixation system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๆ€่ฟช็ถ“็šฎ่„ŠๆคŽๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

c7de9b4bf85928ab9e74f859d195a06e

DHA00601964202

Company Information

United States

Product Details

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

N Orthopedics

N.3070 ๆคŽๅผ“่žบ้‡˜็ณป็ตฑ

import

Dates and Status

Feb 06, 2009

Feb 06, 2029