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“Stryker” CrossFlow Integrated Arthroscopy Pump - Taiwan Registration d06d98e9e361bbcd21a4f18a8182a922

Access comprehensive regulatory information for “Stryker” CrossFlow Integrated Arthroscopy Pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d06d98e9e361bbcd21a4f18a8182a922 and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

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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d06d98e9e361bbcd21a4f18a8182a922
Registration Details
Taiwan FDA Registration: d06d98e9e361bbcd21a4f18a8182a922
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Device Details

“Stryker” CrossFlow Integrated Arthroscopy Pump
TW: “史賽克”整合關節鏡幫浦
Risk Class 2
MD

Registration Details

d06d98e9e361bbcd21a4f18a8182a922

Ministry of Health Medical Device Import No. 036016

DHA05603601603

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N1100 Arthroscopy

Imported from abroad

Dates and Status

Oct 31, 2022

Oct 31, 2027