Taiwan FDA registration 65f75cdccd514f0b570d245ccc987462
"Meku" manual orthopedic surgical instruments (sterilized/unsterilized)
TW: "美酷"手動式骨科手術器械(滅菌/未滅菌)
Taiwan·Risk Class 1·MAKO Surgical Corp.·Registered Apr 25, 2014 – Apr 25, 2029ActiveRegistration details
- Analysis ID
- 65f75cdccd514f0b570d245ccc987462
- Customs Code
- DHA09401409306
Company information
- Manufacturer
- MAKO Surgical Corp.
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 25, 2014
- Expiry Date
- Apr 25, 2029
About this record
Access comprehensive regulatory information for "Meku" manual orthopedic surgical instruments (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65f75cdccd514f0b570d245ccc987462 and manufactured by MAKO Surgical Corp.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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