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“AD-TECH” Subdural Electrode - Taiwan Registration c8e137533931f3a83a3992175211c4b8

Access comprehensive regulatory information for “AD-TECH” Subdural Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8e137533931f3a83a3992175211c4b8 and manufactured by AD-TECH MEDICAL INSTRUMENT CORPORATION. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..

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c8e137533931f3a83a3992175211c4b8
Registration Details
Taiwan FDA Registration: c8e137533931f3a83a3992175211c4b8
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Device Details

“AD-TECH” Subdural Electrode
TW: “艾迪鈦克”皮質電極
Risk Class 2
MD

Registration Details

c8e137533931f3a83a3992175211c4b8

Ministry of Health Medical Device Import No. 030365

DHA05603036501

Company Information

Product Details

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

K Devices for neuroscience

K1310 Cortical electrode

Imported from abroad

Dates and Status

Oct 24, 2017

Oct 24, 2027