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“Tmax” Far Infrared Non-powered Flotation Therapy Mattress (Non Sterile) - Taiwan Registration d42f8fba834e6ecaa09089a23a1ad53d

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 d42f8fba834e6ecaa09089a23a1ad53d 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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d42f8fba834e6ecaa09089a23a1ad53d
Registration Details
Taiwan FDA Registration: d42f8fba834e6ecaa09089a23a1ad53d
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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

d42f8fba834e6ecaa09089a23a1ad53d

Ministry of Health Medical Device Manufacturing 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

Sep 18, 2019

Sep 18, 2024

Cancellation Information

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