Taiwan FDA registration 4aa4f4d73700976075b6bf40e1581b9b

"Fujita" Potential Therapy Device

TW: “藤田” 電位治療器

Taiwan·Risk Class 2·Fujita Health Business Co., Ltd.;; Morita Kogyo Co., Ltd. Mizuki Plant·Registered Aug 07, 2024 – Aug 07, 2029Active

Registration details

Analysis ID: 4aa4f4d73700976075b6bf40e1581b9b

Company information

Manufacturer: Fujita Health Business Co., Ltd.;; Morita Kogyo Co., Ltd. Mizuki Plant
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Fujita Health Business Co., Ltd

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.0001 靜電器(電位治療器)
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Aug 07, 2024
Expiry Date: Aug 07, 2029

About this record

Access comprehensive regulatory information for "Fujita" Potential 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 4aa4f4d73700976075b6bf40e1581b9b and manufactured by Fujita Health Business Co., Ltd.;; Morita Kogyo Co., Ltd. Mizuki Plant. The authorized representative in Taiwan is Fujita Health Business Co., Ltd.

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.