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“Tmax” Far Infrared Non-powered Flotation Therapy Mattress (Non Sterile) - Taiwan Registration 875cee9fe9b267a9b639b26cb029ca11

Access comprehensive regulatory information for “Tmax” Far Infrared Non-powered Flotation Therapy Mattress (Non Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 875cee9fe9b267a9b639b26cb029ca11 and manufactured by TMAXSTRATEGY & MARKETING INC.. The authorized representative in Taiwan is TMAXSTRATEGY & MARKETING INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TMAXSTRATEGY & MARKETING INC., 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.

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875cee9fe9b267a9b639b26cb029ca11
Registration Details
Taiwan FDA Registration: 875cee9fe9b267a9b639b26cb029ca11
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Device Details

“Tmax” Far Infrared Non-powered Flotation Therapy Mattress (Non Sterile)
TW: “堤麥”遠紅外線非動力式治療床墊 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

875cee9fe9b267a9b639b26cb029ca11

Ministry of Health Medical Device Manufacturing Registration No. 007958

Company Information

Taiwan, Province of China

Product Details

J General hospital and personal use equipment

J5150 Non-powered treatment mattress

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2024

Jun 19, 2023

Cancellation Information

Logged out

療效不確實

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