Taiwan FDA registration 601d0574db746bf0f94ea8f89e43ccee
Medtronic Manual Orthopedic Instruments (Sterilization)
TW: “美敦力”手動式骨科手術器械（滅菌）
Taiwan·Risk Class 1·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Jul 16, 2010 – Jul 16, 2025ExpiredRegistration details
- Analysis ID
- 601d0574db746bf0f94ea8f89e43ccee
- Customs Code
- DHA04400899502
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK MANUFACTURING
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
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
- Jul 16, 2010
- Expiry Date
- Jul 16, 2025
About this record
Access comprehensive regulatory information for Medtronic Manual Orthopedic Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 601d0574db746bf0f94ea8f89e43ccee and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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