Taiwan FDA registration 331b0c07ebda25235e19cd927d729276
"Medtronic" neuroendoscope and accessories
TW: “美敦力”神經內視鏡及附件
Taiwan·Risk Class 2·MEDTRONIC NEUROSURGERY·Registered May 02, 2008 – May 02, 2018CancelledRegistration details
- Analysis ID
- 331b0c07ebda25235e19cd927d729276
- Customs Code
- DHA00601884202
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
- May 02, 2008
- Expiry Date
- May 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" neuroendoscope and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 331b0c07ebda25235e19cd927d729276 and manufactured by MEDTRONIC NEUROSURGERY. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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