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“Stryker” Navigation ADAPT/NAV3 Platform - Taiwan Registration c248267bc4f6481a0c14fa7cfe0e925b

Access comprehensive regulatory information for “Stryker” Navigation ADAPT/NAV3 Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c248267bc4f6481a0c14fa7cfe0e925b and manufactured by STRYKER LEIBINGER GMBH & CO.KG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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c248267bc4f6481a0c14fa7cfe0e925b
Registration Details
Taiwan FDA Registration: c248267bc4f6481a0c14fa7cfe0e925b
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Device Details

“Stryker” Navigation ADAPT/NAV3 Platform
TW: “史賽克”手術導航系統平台
Risk Class 2
MD

Registration Details

c248267bc4f6481a0c14fa7cfe0e925b

Ministry of Health Medical Device Import No. 026169

DHA05602616909

Company Information

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 15, 2014

May 15, 2024