Taiwan FDA registration 0b83b2cb408d8e80a8b7fccc52db5cc1
“Medtronic” Nexframe Stereotactic System
TW: “美敦力”奈克斯弗立體定位系統
Taiwan·Risk Class 2·MD·FHC, INC.·Registered May 31, 2017 – May 31, 2027ActiveRegistration details
- Analysis ID
- 0b83b2cb408d8e80a8b7fccc52db5cc1
- License Form
- Ministry of Health Medical Device Import No. 029869
- Customs Code
- DHA05602986900
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)
- K4560 Instrument for stereotaxic use in the nervous system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 31, 2017
- Expiry Date
- May 31, 2027
About this record
Access comprehensive regulatory information for “Medtronic” Nexframe Stereotactic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b83b2cb408d8e80a8b7fccc52db5cc1 and manufactured by FHC, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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