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“CSI” Alternating Pressure Air Flotation Mattress(Non-Sterile) - Taiwan Registration 9395c039e28c2d95531fbd3071a94fee

Access comprehensive regulatory information for “CSI” Alternating Pressure Air Flotation 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 9395c039e28c2d95531fbd3071a94fee and manufactured by CAREMED SUPPLY INC.. The authorized representative in Taiwan is CAREMED SUPPLY INC..

This page provides complete technical specifications, regulatory compliance details. 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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9395c039e28c2d95531fbd3071a94fee
Registration Details
Taiwan FDA Registration: 9395c039e28c2d95531fbd3071a94fee
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Device Details

“CSI” Alternating Pressure Air Flotation Mattress(Non-Sterile)
TW: “繁葵”交替式壓力氣墊床(未滅菌)
Risk Class 1
MD

Registration Details

9395c039e28c2d95531fbd3071a94fee

Ministry of Health Medical Device Manufacturing No. 007452

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".

J General hospital and personal use equipment

J5550 Alternating pressure air mattress

Produced in Taiwan, China

Dates and Status

Sep 26, 2018

Sep 26, 2028