Taiwan FDA registration 3d84b72e7d7ea62903ce818919a606b1
"INT" TRI CELL Alternating Pressure Relief System (Non-Sterile)
TW: "愛恩特"三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 Jan 11, 2011 – Jan 11, 2026ExpiredRegistration details
- Analysis ID
- 3d84b72e7d7ea62903ce818919a606b1
- License Form
- Department of Health Medical Device Manufacturing No. 003297
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 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
- Jan 11, 2011
- Expiry Date
- Jan 11, 2026
About this record
Access comprehensive regulatory information for "INT" TRI CELL Alternating 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 3d84b72e7d7ea62903ce818919a606b1 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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