Taiwan FDA registration e791a419c021881bf6d9e562264e7f6f
“Fustenber” Alternation Pressure-Relief System (Non-Sterile)
TW: “福斯騰”交替防褥瘡氣墊床組(未滅菌)
Taiwan·Risk Class 1·MD·Noble Industrial Co., Ltd. Chiayi Factory·Registered Dec 12, 2018 – Dec 12, 2028ActiveRegistration details
- Analysis ID
- e791a419c021881bf6d9e562264e7f6f
- License Form
- Ministry of Health Medical Device Manufacturing No. 007566
Company information
- Manufacturer
- Noble Industrial Co., Ltd. Chiayi Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- INT MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- 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
Dates and status
- Registration Date
- Dec 12, 2018
- Expiry Date
- Dec 12, 2028
About this record
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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