Taiwan FDA registration a6413a3dd49fa9e23ee7ecb2df2345dc
“Medtronic” Nexframe Passive Headrest
TW: “美敦力”奈克斯弗被動式頭墊
Taiwan·Risk Class 2·MD·FHC, INC.·Registered Jul 11, 2017 – Jul 11, 2027ActiveRegistration details
- Analysis ID
- a6413a3dd49fa9e23ee7ecb2df2345dc
- License Form
- Ministry of Health Medical Device Import No. 029940
- Customs Code
- DHA05602994006
Company information
- Manufacturer
- FHC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K4460 Head fixation for neurosurgery
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 11, 2017
- Expiry Date
- Jul 11, 2027
About this record
Access comprehensive regulatory information for “Medtronic” Nexframe 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 a6413a3dd49fa9e23ee7ecb2df2345dc and manufactured by FHC, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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