Taiwan FDA registration eeb2a3d46847705be3ac100526e67297
“MAKO” RESTORIS MCK Patellofemoral Knee System
TW: “美酷”髕骨股骨人工關節系統
Taiwan·Risk Class 2·MD·MAKO Surgical Corp.·Registered Jul 09, 2014 – Jul 09, 2024ExpiredRegistration details
- Analysis ID
- eeb2a3d46847705be3ac100526e67297
- License Form
- Ministry of Health Medical Device Import No. 026335
- Customs Code
- DHA05602633500
Company information
- Manufacturer
- MAKO Surgical Corp.
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3540 Semi-restrictive knee diaphragmal polymer/metallic cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 09, 2014
- Expiry Date
- Jul 09, 2024
About this record
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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