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“Medtronic” Nexprobe Image-guided Probe - Taiwan Registration 12970771cabcd6afbd2bab2bdcc9554f

Access comprehensive regulatory information for “Medtronic” Nexprobe Image-guided Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12970771cabcd6afbd2bab2bdcc9554f 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.

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12970771cabcd6afbd2bab2bdcc9554f
Registration Details
Taiwan FDA Registration: 12970771cabcd6afbd2bab2bdcc9554f
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Device Details

“Medtronic” Nexprobe Image-guided Probe
TW: “美敦力”奈克斯柏影像導引探針
Risk Class 2
MD

Registration Details

12970771cabcd6afbd2bab2bdcc9554f

Ministry of Health Medical Device Import No. 029738

DHA05602973801

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 23, 2017

May 23, 2027