Taiwan FDA registration 7d569bc16a0dcfcd91b3880330adce76
"Medtronic" power system equipment
TW: “美敦力”動力系統器械
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered May 27, 2019 – May 27, 2029ActiveRegistration details
- Analysis ID
- 7d569bc16a0dcfcd91b3880330adce76
- Customs Code
- DHA05603267701
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4310 Power Simplicity Head, Steel, Rings and Accessories
- Import Information
- import
Dates and status
- Registration Date
- May 27, 2019
- Expiry Date
- May 27, 2029
About this record
Access comprehensive regulatory information for "Medtronic" power system equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d569bc16a0dcfcd91b3880330adce76 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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