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“Stryker” AIR+ All-Inside Meniscal Repair System - Taiwan Registration c6e7866a5595f754b5dbca107a9e9a2e

Access comprehensive regulatory information for “Stryker” AIR+ All-Inside Meniscal Repair System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6e7866a5595f754b5dbca107a9e9a2e and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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c6e7866a5595f754b5dbca107a9e9a2e
Registration Details
Taiwan FDA Registration: c6e7866a5595f754b5dbca107a9e9a2e
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Device Details

“Stryker” AIR+ All-Inside Meniscal Repair System
TW: “史賽克”艾爾半月板修復系統
Risk Class 2
MD

Registration Details

c6e7866a5595f754b5dbca107a9e9a2e

Ministry of Health Medical Device Import No. 035071

DHA05603507106

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3040 Smooth or threaded metal bone fixation

Imported from abroad

Dates and Status

Nov 29, 2021

Nov 29, 2026