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"Funai" mini low frequency - Taiwan Registration 91b6905d1326dbaef4994c67f0b68ff3

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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91b6905d1326dbaef4994c67f0b68ff3
Registration Details
Taiwan FDA Registration: 91b6905d1326dbaef4994c67f0b68ff3
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Device Details

"Funai" mini low frequency
TW: "่ˆนไบ•" ่ฟทไฝ ไฝŽ้€ฑๆณข
Risk Class 2

Registration Details

91b6905d1326dbaef4994c67f0b68ff3

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

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Domestic

Dates and Status

May 14, 2022

May 14, 2027