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“Fustenber” Four ways Alternating Pressure-Relif System(Non-Sterile) - Taiwan Registration c862fe2aa6d4dc4c4e460751deb8faac

Access comprehensive regulatory information for “Fustenber” Four ways Alternating Pressure-Relif 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 c862fe2aa6d4dc4c4e460751deb8faac and manufactured by Noble Industrial Co., Ltd. Chiayi Factory. The authorized representative in Taiwan is Noble Industrial Co., Ltd. Chiayi Factory.

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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c862fe2aa6d4dc4c4e460751deb8faac
Registration Details
Taiwan FDA Registration: c862fe2aa6d4dc4c4e460751deb8faac
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Device Details

“Fustenber” Four ways Alternating Pressure-Relif System(Non-Sterile)
TW: “福斯騰”四管交替防褥瘡氣墊床組(未滅菌)
Risk Class 1
MD

Registration Details

c862fe2aa6d4dc4c4e460751deb8faac

Ministry of Health Medical Device Manufacturing No. 009146

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment "Alternating pressure air mattress (J.5550)" level identification range.

J General hospital and personal use equipment

J5550 Alternating pressure air mattress

Produced in Taiwan, China; GMP

Dates and Status

Jun 24, 2021

Jun 24, 2026