Taiwan FDA registration 9d01f6b23711ee24c3bda7a34dfbbeb6
"Medtronic" stimulation test lead set
TW: “美敦力”刺激測試導線組
Taiwan·Risk Class 2·MEDTRONIC NEUROMODULATION·Registered Apr 01, 2013 – Apr 01, 2023CancelledRegistration details
- Analysis ID
- 9d01f6b23711ee24c3bda7a34dfbbeb6
- Customs Code
- DHA00602482909
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION
- 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.5880 Implantable spinal cord stimulator for pain relief
- Import Information
- import
Dates and status
- Registration Date
- Apr 01, 2013
- Expiry Date
- Apr 01, 2023
- Cancellation Date
- Aug 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Medtronic" stimulation test lead set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d01f6b23711ee24c3bda7a34dfbbeb6 and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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