Taiwan FDA registration fab4aa064920c4f32c96c1b59342c4b2
"Medtronic" Nexford passive headrest
TW: “美敦力”奈克斯弗被動式頭墊
Taiwan·Risk Class 2·MEDTRONIC NEUROMODULATION·Registered May 21, 2010 – May 21, 2015CancelledRegistration details
- Analysis ID
- fab4aa064920c4f32c96c1b59342c4b2
- Customs Code
- DHA00602104308
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.4460 神經外科用頭固定物
- Import Information
- import
Dates and status
- Registration Date
- May 21, 2010
- Expiry Date
- May 21, 2015
- Cancellation Date
- Sep 11, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Medtronic" Nexford passive headrest in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fab4aa064920c4f32c96c1b59342c4b2 and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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