“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).
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
eeb2a3d46847705be3ac100526e67297
Ministry of Health Medical Device Import No. 026335
DHA05602633500
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

