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“Cayenne” AperFix II Tibial System - Taiwan Registration a9f8da0dd8871656c1d2b789fc1b9e6d

Access comprehensive regulatory information for “Cayenne” AperFix II Tibial System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9f8da0dd8871656c1d2b789fc1b9e6d and manufactured by Cayenne Medical, Inc.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

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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a9f8da0dd8871656c1d2b789fc1b9e6d
Registration Details
Taiwan FDA Registration: a9f8da0dd8871656c1d2b789fc1b9e6d
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Device Details

“Cayenne” AperFix II Tibial System
TW: “凱燕”艾波斐II脛骨系統
Risk Class 2
MD

Registration Details

a9f8da0dd8871656c1d2b789fc1b9e6d

Ministry of Health Medical Device Import No. 036679

DHA05603667902

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

Jul 26, 2023

Jul 26, 2028