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“Fustenber” Alternation Pressure-Relief System (Non-Sterile) - Taiwan Registration e791a419c021881bf6d9e562264e7f6f

Access comprehensive regulatory information for “Fustenber” Alternation Pressure-Relief System (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 e791a419c021881bf6d9e562264e7f6f and manufactured by Noble Industrial Co., Ltd. Chiayi Factory. The authorized representative in Taiwan is INT MEDICAL CO., LTD..

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e791a419c021881bf6d9e562264e7f6f
Registration Details
Taiwan FDA Registration: e791a419c021881bf6d9e562264e7f6f
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Device Details

“Fustenber” Alternation Pressure-Relief System (Non-Sterile)
TW: “福斯騰”交替防褥瘡氣墊床組(未滅菌)
Risk Class 1
MD

Registration Details

e791a419c021881bf6d9e562264e7f6f

Ministry of Health Medical Device Manufacturing No. 007566

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

Dec 12, 2018

Dec 12, 2028