Taiwan FDA registration 3a57767510f4fce59cd829ea06d270b2
"Medtronic" Radiant Patient Program Controller
TW: "美敦力"艾璀病患程控儀
Taiwan·Risk Class 3·MEDTRONIC NEUROMODULATION·Registered Dec 15, 2006 – Dec 15, 2011CancelledRegistration details
- Analysis ID
- 3a57767510f4fce59cd829ea06d270b2
- Customs Code
- DHA00601751406
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.5840 Implantable intracranial/subdermal stimulator for pain relief
- Import Information
- import
Dates and status
- Registration Date
- Dec 15, 2006
- Expiry Date
- Dec 15, 2011
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" Radiant Patient Program Controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3a57767510f4fce59cd829ea06d270b2 and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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