Taiwan FDA registration 30b97ee7656ec9cd51bd9f9a2f8994b0

"Wanmei" magnetic wave therapy device

TW: “萬美” 磁波治療器

Taiwan·Risk Class 2·K1MED Co., Ltd.·Registered Jan 15, 2024 – Jan 15, 2029Active

Registration details

Analysis ID: 30b97ee7656ec9cd51bd9f9a2f8994b0
Customs Code: DHA05603690202

Company information

Manufacturer: K1MED Co., Ltd.
Manufacturer Country: Korea, Republic of
Authorized Representative: SERVICETECH INTERNATIONAL INC.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): K Neuroscience;;O Physical Medical Sciences
Product Type (Level 2): K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator
Import Information: import

Dates and status

Registration Date: Jan 15, 2024
Expiry Date: Jan 15, 2029

About this record

Access comprehensive regulatory information for "Wanmei" magnetic wave therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30b97ee7656ec9cd51bd9f9a2f8994b0 and manufactured by K1MED Co., Ltd.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..

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