Taiwan FDA registration 4ab631268ab9f08e9002ad6d5f36b1ae
“Medtronic” Restore Clinician Programmer Application
TW: “美敦力” 瑞斯特程控儀應用程式
Taiwan·Risk Class 2·MD·MEDTRONIC NEUROMODULATION·Registered Dec 22, 2020 – Dec 22, 2025ExpiredRegistration details
- Analysis ID
- 4ab631268ab9f08e9002ad6d5f36b1ae
- License Form
- Ministry of Health Medical Device Import No. 034131
- Customs Code
- DHA05603413106
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- A71100
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5880 Implantable spinal cord stimulator for pain relief
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 22, 2020
- Expiry Date
- Dec 22, 2025
About this record
Access comprehensive regulatory information for “Medtronic” Restore Clinician Programmer Application in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ab631268ab9f08e9002ad6d5f36b1ae and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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