Taiwan FDA registration a7b6216f6e8529bd7c0a3a2478149682
“LKC” Visual Electrodiagnostic Device
TW: “樂可視”視覺電子診斷系統
Taiwan·Risk Class 2·MD·LKC TECHNOLOGIES, INC.·Registered Aug 22, 2018 – Aug 22, 2028ActiveRegistration details
- Analysis ID
- a7b6216f6e8529bd7c0a3a2478149682
- License Form
- Ministry of Health Medical Device Import No. 031567
- Customs Code
- DHA05603156702
Company information
- Manufacturer
- LKC TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
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)
- K1890 Evoked reactive photostimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 22, 2018
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for “LKC” Visual Electrodiagnostic Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a7b6216f6e8529bd7c0a3a2478149682 and manufactured by LKC TECHNOLOGIES, INC.. The authorized representative in Taiwan is CLINICO INC..
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