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“SANYOSEIKO” Pain and Sensory Evaluation System - Taiwan Registration a8064ae6851e6a84b4fcb3607a0097e6

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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a8064ae6851e6a84b4fcb3607a0097e6
Registration Details
Taiwan FDA Registration: a8064ae6851e6a84b4fcb3607a0097e6
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Device Details

“SANYOSEIKO” Pain and Sensory Evaluation System
TW: “山陽精工”痛覺知覺測量記錄裝置
Risk Class 2
MD

Registration Details

a8064ae6851e6a84b4fcb3607a0097e6

Ministry of Health Medical Device Import No. 033388

DHA05603338802

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

K Devices for neuroscience

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Imported from abroad

Dates and Status

Mar 14, 2020

Mar 14, 2025