Taiwan FDA registration c862fe2aa6d4dc4c4e460751deb8faac
“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)
Taiwan·Risk Class 1·MD·Noble Industrial Co., Ltd. Chiayi Factory·Registered Jun 24, 2021 – Jun 24, 2026ExpiredRegistration details
- Analysis ID
- c862fe2aa6d4dc4c4e460751deb8faac
- License Form
- Ministry of Health Medical Device Manufacturing No. 009146
Company information
- Manufacturer
- Noble Industrial Co., Ltd. Chiayi Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Noble Industrial Co., Ltd. Chiayi Factory
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment "Alternating pressure air mattress (J.5550)" level identification range.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5550 Alternating pressure air mattress
- Import Information
- Produced in Taiwan, China; GMP
Dates and status
- Registration Date
- Jun 24, 2021
- Expiry Date
- Jun 24, 2026
About this record
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.
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