Taiwan FDA registration ff3df7723c97524c84292674f77d451d
"Meiku" stereotaxic robotic arm assisted joint replacement surgery system
TW: “美酷”立體定位機器臂輔助關節置換手術系統
Taiwan·Risk Class 2·MAKO Surgical Corp.·Registered Jul 31, 2024 – Jul 31, 2029ActiveRegistration details
- Analysis ID
- ff3df7723c97524c84292674f77d451d
- Customs Code
- DHA05603734004
Company information
- Manufacturer
- MAKO Surgical Corp.
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4560 Instruments for stereotaxic use of the nervous system
- Import Information
- import
Dates and status
- Registration Date
- Jul 31, 2024
- Expiry Date
- Jul 31, 2029
About this record
Access comprehensive regulatory information for "Meiku" stereotaxic robotic arm assisted joint replacement surgery system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff3df7723c97524c84292674f77d451d and manufactured by MAKO Surgical Corp.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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