Taiwan FDA registration e6e91c5fb46dc632797b640fa906d346
"Medtronic" neuroendoscopic shunt placement group
TW: “美敦力”神經內視鏡分流置放組
Taiwan·Risk Class 2·MEDTRONIC NEUROSURGERY·Registered Jun 02, 2008 – Jun 02, 2018CancelledRegistration details
- Analysis ID
- e6e91c5fb46dc632797b640fa906d346
- Customs Code
- DHA00601888405
Company information
- Manufacturer
- MEDTRONIC NEUROSURGERY
- 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.1480 神經學科用內視鏡
- Import Information
- import
Dates and status
- Registration Date
- Jun 02, 2008
- Expiry Date
- Jun 02, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" neuroendoscopic shunt placement group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e6e91c5fb46dc632797b640fa906d346 and manufactured by MEDTRONIC NEUROSURGERY. 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