Taiwan FDA registration edbcb2f775f64d923ad22bd60db87640
“Cadwell” Intraoperative Monitor
TW: “凱特維爾”肌電圖/誘發電位檢查儀
Taiwan·Risk Class 2·MD·CADWELL INDUSTRIES, INC.·Registered May 30, 2018 – May 30, 2028ActiveRegistration details
- Analysis ID
- edbcb2f775f64d923ad22bd60db87640
- License Form
- Ministry of Health Medical Device Import No. 030910
- Customs Code
- DHA05603091000
Company information
- Manufacturer
- CADWELL INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
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)
- K1870 Evoked reactive electrical stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 30, 2018
- Expiry Date
- May 30, 2028
About this record
Access comprehensive regulatory information for “Cadwell” Intraoperative Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number edbcb2f775f64d923ad22bd60db87640 and manufactured by CADWELL INDUSTRIES, INC.. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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