Taiwan FDA registration 91b6905d1326dbaef4994c67f0b68ff3

"Funai" mini low frequency

TW: "船井" 迷你低週波

Taiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered May 14, 2022 – May 14, 2027Active

Registration details

Analysis ID: 91b6905d1326dbaef4994c67f0b68ff3

Company information

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

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: Domestic

Dates and status

Registration Date: May 14, 2022
Expiry Date: May 14, 2027

About this record

Access comprehensive regulatory information for "Funai" mini low frequency in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91b6905d1326dbaef4994c67f0b68ff3 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is Hongtai Enterprise Co., Ltd. Rende Factory.

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