Taiwan FDA registration 836db17b883782d5a64a98de9b023e71
“Medtronic” Intercept Patient Programmer
TW: “美敦力”因特賽病患程控儀
Registration details
- Analysis ID
- 836db17b883782d5a64a98de9b023e71
- License Form
- Ministry of Health Medical Device Import No. 025984
- Customs Code
- DHA05602598406
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- K Devices for neuroscience
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 03, 2014
- Expiry Date
- Apr 03, 2024
- Cancellation Date
- Apr 29, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Medtronic” Intercept Patient Programmer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 836db17b883782d5a64a98de9b023e71 and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices