Pure Global

“Medtronic” Nexframe Stereotactic System - Taiwan Registration 0b83b2cb408d8e80a8b7fccc52db5cc1

Access comprehensive regulatory information for “Medtronic” Nexframe Stereotactic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b83b2cb408d8e80a8b7fccc52db5cc1 and manufactured by FHC, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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
0b83b2cb408d8e80a8b7fccc52db5cc1
Registration Details
Taiwan FDA Registration: 0b83b2cb408d8e80a8b7fccc52db5cc1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Medtronic” Nexframe Stereotactic System
TW: “美敦力”奈克斯弗立體定位系統
Risk Class 2
MD

Registration Details

0b83b2cb408d8e80a8b7fccc52db5cc1

Ministry of Health Medical Device Import No. 029869

DHA05602986900

Company Information

United States

Product Details

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

K Devices for neuroscience

K4560 Instrument for stereotaxic use in the nervous system

Imported from abroad

Dates and Status

May 31, 2017

May 31, 2027