Taiwan FDA registration 19b42cc9aa72c4b8eeb5cf526d222b2f

"Live" transcutaneous electrical stimulation therapy device

TW: “活機”經皮電刺激治療器

Taiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Jul 10, 2008 – Jul 10, 2028Active

Registration details

Analysis ID: 19b42cc9aa72c4b8eeb5cf526d222b2f
Customs Code: DHY00500247602

Company information

Manufacturer: Hongtai Enterprise Co., Ltd. Rende Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TRANSMISSION INTERNATIONAL TECHNOLOGY CO.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order. Performance and imitation order changes: For details, please refer to the Chinese copy of the imitation order (the original 97.7.21 approved copy of the imitation order and label approval will be recycled and invalidated).
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Jul 10, 2008
Expiry Date: Jul 10, 2028

About this record

Access comprehensive regulatory information for "Live" transcutaneous electrical stimulation 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 19b42cc9aa72c4b8eeb5cf526d222b2f and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is TRANSMISSION INTERNATIONAL TECHNOLOGY CO..

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