Taiwan FDA registration bf3c226f2c8d4ea05347887b2ea89079
Medtronic Manual Orthopedic Surgical Instruments (Unsterilized)
TW: “美敦力”手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Aug 27, 2009 – Aug 27, 2029ActiveRegistration details
- Analysis ID
- bf3c226f2c8d4ea05347887b2ea89079
- Customs Code
- DHA04400801201
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC.
- 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
- QMS/QSD
Dates and status
- Registration Date
- Aug 27, 2009
- Expiry Date
- Aug 27, 2029
About this record
Access comprehensive regulatory information for Medtronic Manual Orthopedic Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf3c226f2c8d4ea05347887b2ea89079 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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