Taiwan FDA registration de9f8b12305df4cceb61d4b6fea94316

"Funai" low week wave therapy device

TW: "船井" 低週波治療器
Taiwan flagTaiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Aug 15, 2003 – Aug 12, 2016Cancelled
Registration details
Analysis ID
de9f8b12305df4cceb61d4b6fea94316
Customs Code
DHY00500101602
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
HOME CARE TECHNOLOGY CO., LTD.
Product details
Product Type (Level 1)
K Neuroscience
Import Information
Domestic
Dates and status
Registration Date
Aug 15, 2003
Expiry Date
Aug 12, 2016
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
Companies making similar products

Top companies providing products similar to ""Funai" low week wave therapy device"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Funai" low week wave 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 de9f8b12305df4cceb61d4b6fea94316 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is HOME CARE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hongtai Enterprise Co., Ltd. Rende Factory, and 1 recent registrations in the same category. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations