“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.
Device Details
Registration Details
c6e7866a5595f754b5dbca107a9e9a2e
Ministry of Health Medical Device Import No. 035071
DHA05603507106
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

