Taiwan FDA registration a8064ae6851e6a84b4fcb3607a0097e6
“SANYOSEIKO” Pain and Sensory Evaluation System
TW: “山陽精工”痛覺知覺測量記錄裝置
Taiwan·Risk Class 2·MD·SANYOSEIKO CO., LTD.·Registered Mar 14, 2020 – Mar 14, 2025ExpiredRegistration details
- Analysis ID
- a8064ae6851e6a84b4fcb3607a0097e6
- License Form
- Ministry of Health Medical Device Import No. 033388
- Customs Code
- DHA05603338802
Company information
- Manufacturer
- SANYOSEIKO CO., LTD.
- Manufacturer Country
- Japan
- 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
- Mar 14, 2020
- Expiry Date
- Mar 14, 2025
About this record
Access comprehensive regulatory information for “SANYOSEIKO” Pain and Sensory Evaluation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a8064ae6851e6a84b4fcb3607a0097e6 and manufactured by SANYOSEIKO CO., LTD.. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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