Taiwan FDA registration 12970771cabcd6afbd2bab2bdcc9554f
“Medtronic” Nexprobe Image-guided Probe
TW: “美敦力”奈克斯柏影像導引探針
Taiwan·Risk Class 2·MD·FHC, INC.·Registered May 23, 2017 – May 23, 2027ActiveRegistration details
- Analysis ID
- 12970771cabcd6afbd2bab2bdcc9554f
- License Form
- Ministry of Health Medical Device Import No. 029738
- Customs Code
- DHA05602973801
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 23, 2017
- Expiry Date
- May 23, 2027
About this record
Access comprehensive regulatory information for “Medtronic” Nexprobe Image-guided Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12970771cabcd6afbd2bab2bdcc9554f and manufactured by FHC, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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