Taiwan FDA registration d42f8fba834e6ecaa09089a23a1ad53d

“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)
Taiwan flagTaiwan·Risk Class 1·MD·TMAXSTRATEGY & MARKETING INC.·Registered Sep 18, 2019 – Sep 18, 2024Cancelled
Registration details
Analysis ID
d42f8fba834e6ecaa09089a23a1ad53d
License Form
Ministry of Health Medical Device Manufacturing No. 007958
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TMAXSTRATEGY & MARKETING INC.
Product details
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J5150 Non-powered treatment mattress
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Sep 18, 2019
Expiry Date
Sep 18, 2024
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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