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“Medtronic” Nexframe Passive Headrest - Taiwan Registration a6413a3dd49fa9e23ee7ecb2df2345dc

Access comprehensive regulatory information for “Medtronic” Nexframe Passive Headrest in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a6413a3dd49fa9e23ee7ecb2df2345dc 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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a6413a3dd49fa9e23ee7ecb2df2345dc
Registration Details
Taiwan FDA Registration: a6413a3dd49fa9e23ee7ecb2df2345dc
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Device Details

“Medtronic” Nexframe Passive Headrest
TW: “美敦力”奈克斯弗被動式頭墊
Risk Class 2
MD

Registration Details

a6413a3dd49fa9e23ee7ecb2df2345dc

Ministry of Health Medical Device Import No. 029940

DHA05602994006

Company Information

United States

Product Details

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

K Devices for neuroscience

K4460 Head fixation for neurosurgery

Imported from abroad

Dates and Status

Jul 11, 2017

Jul 11, 2027