Taiwan FDA registration 3bb835d5165b9128e17083c7b31ba482

"REMDE" magnetic wave therapy

TW: “瑞美德” 磁波治療器

Taiwan·Risk Class 2·Remed Co., Ltd.·Registered May 01, 2024 – May 01, 2029Active

Registration details

Analysis ID: 3bb835d5165b9128e17083c7b31ba482
Customs Code: DHA05603698101

Company information

Manufacturer: Remed 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: May 01, 2024
Expiry Date: May 01, 2029

About this record

Access comprehensive regulatory information for "REMDE" magnetic wave therapy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3bb835d5165b9128e17083c7b31ba482 and manufactured by Remed Co., Ltd.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..

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