Taiwan FDA registration 38d407bd49dd5b582c6d82613cb1d087

Meisi Medical Stress Relief Mattress (Unsterilized)

TW: 美思醫療減壓床墊(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Qiaofu Medical Equipment Co., Ltd.; Meisi Technology Co., Ltd·Registered Apr 28, 2021 – Apr 28, 2026Cancelled
Registration details
Analysis ID
38d407bd49dd5b582c6d82613cb1d087
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Cognito Health Inc.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5150 Non-powered floating therapy mattress
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Apr 28, 2021
Expiry Date
Apr 28, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for Meisi Medical Stress Relief Mattress (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38d407bd49dd5b582c6d82613cb1d087 and manufactured by Qiaofu Medical Equipment Co., Ltd.; Meisi Technology Co., Ltd. The authorized representative in Taiwan is Cognito Health Inc..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Max Technology Co., Ltd.;; Qiao Fu Medical Equipment Co., Ltd, 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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