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“MAKO” RESTORIS MCK Patellofemoral Knee System - Taiwan Registration eeb2a3d46847705be3ac100526e67297

Access comprehensive regulatory information for “MAKO” RESTORIS MCK Patellofemoral Knee System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eeb2a3d46847705be3ac100526e67297 and manufactured by MAKO Surgical Corp.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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eeb2a3d46847705be3ac100526e67297
Registration Details
Taiwan FDA Registration: eeb2a3d46847705be3ac100526e67297
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Device Details

“MAKO” RESTORIS MCK Patellofemoral Knee System
TW: “美酷”髕骨股骨人工關節系統
Risk Class 2
MD

Registration Details

eeb2a3d46847705be3ac100526e67297

Ministry of Health Medical Device Import No. 026335

DHA05602633500

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3540 Semi-restrictive knee diaphragmal polymer/metallic cement compound

Imported from abroad

Dates and Status

Jul 09, 2014

Jul 09, 2024