Taiwan FDA registration 696bdd50a8c453fecc16fb9184a97d04
“Medtronic” Spine Navigated Instruments
TW: “美敦力”脊椎導航器械
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered May 28, 2018 – May 28, 2023ExpiredRegistration details
- Analysis ID
- 696bdd50a8c453fecc16fb9184a97d04
- License Form
- Ministry of Health Medical Device Import No. 031151
- Customs Code
- DHA05603115100
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 Devices for neuroscience
- Product Type (Level 2)
- K4560 Instrument for stereotaxic use in the nervous system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2018
- Expiry Date
- May 28, 2023
About this record
Access comprehensive regulatory information for “Medtronic” Spine Navigated Instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 696bdd50a8c453fecc16fb9184a97d04 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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