Pure Global

“Medtronic” Prestige LP Cervical Disc System - Taiwan Registration fa3930d84a2e67a227ccc94253d89cb9

Access comprehensive regulatory information for “Medtronic” Prestige LP Cervical Disc System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa3930d84a2e67a227ccc94253d89cb9 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
fa3930d84a2e67a227ccc94253d89cb9
Registration Details
Taiwan FDA Registration: fa3930d84a2e67a227ccc94253d89cb9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Medtronic” Prestige LP Cervical Disc System
TW: “美敦力”貝堤頸椎椎間盤系統
Risk Class 2
MD

Registration Details

fa3930d84a2e67a227ccc94253d89cb9

Ministry of Health Medical Device Import No. 025419

DHA05602541901

Company Information

United States

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Sep 16, 2013

Sep 16, 2023